Überblick über die Statistik des Gehaltsniveaus für "Global Content Writer in Deutschland"

Location: Belgium - Hybrid (2 days in office) Schedule: Full-time, Permanent CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Medical Writing Director.   The Medical Writing Director will function as a Lead Medical Writer for a variety of regulatory writing deliverables; and will prepare assigned documents in accordance with the internal/client SOPs and health authority requirements as per the agreed timelines. This individual will conduct a senior review of medical writing deliverables (CSR, IBs, Protocols, etc.), negotiate timelines, and discuss and resolve clients' comments. This role will provide written and verbal feedback to the internal team and clients when appropriate. She/he will keep abreast of current medical writing and regulatory knowledge, including Good Clinical Practice (GCP)/AMWA/EMWA along with developments and advances in clinical drug development. Join our team and help us deliver clinical trials that will improve patients' lives.   Main Job Tasks and Responsibilities: Takes a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating, and adhering to timelines, organizing document reviews, and communicating directly with the clients.Plans and organizes workload for assigned projects and tasks: identifies project needs, tracks timelines, and implements clients' requests.Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.Presents on Medical Writing processes at full-service bid defense meetings.Develops and delivers training to the global team in various aspects of medical writing.Facilitates project budgeting activities for the medical writing scope by collaborating with the BD team.Creates and maintains standard operating procedures and work instructions to prepare and maintain compliant medical writing deliverables.Oversight of a portfolio of clients.Liaison with assigned clients throughout the lifecycle of a project or program of projects to establish requirements and processes, monitor quality, and capitalize on business development opportunities.Provides scientific and technical guidance to the client and Medical Writers.Provides medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.Keeps Medical Writing senior management informed of project status and any issues that affect document quality, timelines, and adherence to contractual obligations.Serves as the primary client contact and Medical Writing representative on assigned project teams, providing support to the Project for developing efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Education and Experience:At minimum a Bachelor's degree or equivalent in medical-related field or life science. Post-graduate degree preferred.At least 10 years of experience as a clinical/regulatory Medical Writer with good clinical/scientific writing skills.Experience working on end-to-end CSR, IBs, and Protocols across different TAs is mandatory. Experience in DSUR will be considered an added advantage.An understanding of the drug development process.Broad experience managing the medical writing responsibilities associated with multiple studies at various stages.Experience in interacting with cross-functional study team members. Specific Role Requirements and Skills:Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research, and medical writing standards.Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; be attentive to details.Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within an agreed client and regulatory timelines; monitored and communicated progress against milestones; escalate complex issues appropriately.Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members.Read, write, and speak fluent English, excellent verbal, and written communication skills.Able to assimilate and summarize large volumes of scientific data accurately, clearly, and concisely.Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Outlook.Be able to juggle multiple priorities and adapt quickly to new situations and new project demands.Culturally aware and able to work comfortably within a global team. The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected]@cromsource.com for more information. Who will you be working for?  About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                  Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates. About TalentSource Life Sciences  TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously. CROMSOURCE is an equal opportunity employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status. Keywords: Medical Writing Director, Director of Medical Writing, Director Medical Writer, Director Medical Writing, Clinical Trials, CEP, CER, PMSR, PSUR, SOPs, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated, Clinical Evaluation Reports, medical writing, clinical study, pharmacology, clinical writing.Skills: Medical Writer, CER, clinical trials, CRO, Medical Writing, Outsourcing, PharmacologyLocation: BelgiumShare: LinkedIn Facebook Twitter Email

Location: Netherlands - Hybrid (2 days in office) Schedule: Full-time, Permanent CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Medical Writing Director.   The Medical Writing Director will function as a Lead Medical Writer for a variety of regulatory writing deliverables; and will prepare assigned documents in accordance with the internal/client SOPs and health authority requirements as per the agreed timelines. This individual will conduct a senior review of medical writing deliverables (CSR, IBs, Protocols, etc.), negotiate timelines, and discuss and resolve clients' comments. This role will provide written and verbal feedback to the internal team and clients when appropriate. She/he will keep abreast of current medical writing and regulatory knowledge, including Good Clinical Practice (GCP)/AMWA/EMWA along with developments and advances in clinical drug development. Join our team and help us deliver clinical trials that will improve patients' lives.   Main Job Tasks and Responsibilities: Takes a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating, and adhering to timelines, organizing document reviews, and communicating directly with the clients.Plans and organizes workload for assigned projects and tasks: identifies project needs, tracks timelines, and implements clients' requests.Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.Presents on Medical Writing processes at full-service bid defense meetings.Develops and delivers training to the global team in various aspects of medical writing.Facilitates project budgeting activities for the medical writing scope by collaborating with the BD team.Creates and maintains standard operating procedures and work instructions to prepare and maintain compliant medical writing deliverables.Oversight of a portfolio of clients.Liaison with assigned clients throughout the lifecycle of a project or program of projects to establish requirements and processes, monitor quality, and capitalize on business development opportunities.Provides scientific and technical guidance to the client and Medical Writers.Provides medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.Keeps Medical Writing senior management informed of project status and any issues that affect document quality, timelines, and adherence to contractual obligations.Serves as the primary client contact and Medical Writing representative on assigned project teams, providing support to the Project for developing efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Education and Experience:At minimum a Bachelor's degree or equivalent in medical-related field or life science. Post-graduate degree preferred.At least 10 years of experience as a clinical/regulatory Medical Writer with good clinical/scientific writing skills.Experience working on end-to-end CSR, IBs, and Protocols across different TAs is mandatory. Experience in DSUR will be considered an added advantage.An understanding of the drug development process.Broad experience managing the medical writing responsibilities associated with multiple studies at various stages.Experience in interacting with cross-functional study team members. Specific Role Requirements and Skills:Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research, and medical writing standards.Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; be attentive to details.Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within an agreed client and regulatory timelines; monitored and communicated progress against milestones; escalate complex issues appropriately.Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members.Read, write, and speak fluent English, excellent verbal, and written communication skills.Able to assimilate and summarize large volumes of scientific data accurately, clearly, and concisely.Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Outlook.Be able to juggle multiple priorities and adapt quickly to new situations and new project demands.Culturally aware and able to work comfortably within a global team. The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected]@cromsource.com for more information. Who will you be working for?  About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                  Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates. About TalentSource Life Sciences  TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously. CROMSOURCE is an equal opportunity employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status. Keywords: Medical Writing Director, Director of Medical Writing, Director Medical Writer, Director Medical Writing, Clinical Trials, CEP, CER, PMSR, PSUR, SOPs, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated, Clinical Evaluation Reports, medical writing, clinical study, pharmacology, clinical writingSkills: Medical Writer, CER, clinical trials, CRO, Medical Writing, Outsourcing, PharmacologyLocation: NetherlandsShare: LinkedIn Facebook Twitter Email

Location: Germany - Hybrid (2 days in office) Schedule: Full-time, Permanent CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Medical Writing Director.   The Medical Writing Director will function as a Lead Medical Writer for a variety of regulatory writing deliverables; and will prepare assigned documents in accordance with the internal/client SOPs and health authority requirements as per the agreed timelines. This individual will conduct a senior review of medical writing deliverables (CSR, IBs, Protocols, etc.), negotiate timelines, and discuss and resolve clients' comments. This role will provide written and verbal feedback to the internal team and clients when appropriate. She/he will keep abreast of current medical writing and regulatory knowledge, including Good Clinical Practice (GCP)/AMWA/EMWA along with developments and advances in clinical drug development. Join our team and help us deliver clinical trials that will improve patients' lives.   Main Job Tasks and Responsibilities: Takes a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating, and adhering to timelines, organizing document reviews, and communicating directly with the clients.Plans and organizes workload for assigned projects and tasks: identifies project needs, tracks timelines, and implements clients' requests.Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.Presents on Medical Writing processes at full-service bid defense meetings.Develops and delivers training to the global team in various aspects of medical writing.Facilitates project budgeting activities for the medical writing scope by collaborating with the BD team.Creates and maintains standard operating procedures and work instructions to prepare and maintain compliant medical writing deliverables.Oversight of a portfolio of clients.Liaison with assigned clients throughout the lifecycle of a project or program of projects to establish requirements and processes, monitor quality, and capitalize on business development opportunities.Provides scientific and technical guidance to the client and Medical Writers.Provides medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.Keeps Medical Writing senior management informed of project status and any issues that affect document quality, timelines, and adherence to contractual obligations.Serves as the primary client contact and Medical Writing representative on assigned project teams, providing support to the Project for developing efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Education and Experience:At minimum a Bachelor's degree or equivalent in medical-related field or life science. Post-graduate degree preferred.At least 10 years of experience as a clinical/regulatory Medical Writer with good clinical/scientific writing skills.Experience working on end-to-end CSR, IBs, and Protocols across different TAs is mandatory. Experience in DSUR will be considered an added advantage.An understanding of the drug development process.Broad experience managing the medical writing responsibilities associated with multiple studies at various stages.Experience in interacting with cross-functional study team members. Specific Role Requirements and Skills:Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research, and medical writing standards.Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; be attentive to details.Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within an agreed client and regulatory timelines; monitored and communicated progress against milestones; escalate complex issues appropriately.Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members.Read, write, and speak fluent English, excellent verbal, and written communication skills.Able to assimilate and summarize large volumes of scientific data accurately, clearly, and concisely.Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Outlook.Be able to juggle multiple priorities and adapt quickly to new situations and new project demands.Culturally aware and able to work comfortably within a global team. The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected]@cromsource.com for more information. Who will you be working for?  About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                   Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates. About TalentSource Life Sciences  TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously. CROMSOURCE is an equal opportunity employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status. Keywords: Medical Writing Director, Director of Medical Writing, Director Medical Writer, Director Medical Writing, Clinical Trials, CEP, CER, PMSR, PSUR, SOPs, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated, Clinical Evaluation Reports, medical writing, clinical study, pharmacology, clinical writing.Skills: Medical Writer, CER, clinical trials, CRO, Outsourcing, PharmacologyLocation: GermanyShare: LinkedIn Facebook Twitter Email

Location: United Kingdom - Hybrid (2 days in office) Schedule: Full-time, Permanent CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Medical Writing Director.   The Medical Writing Director will function as a Lead Medical Writer for a variety of regulatory writing deliverables; and will prepare assigned documents in accordance with the internal/client SOPs and health authority requirements as per the agreed timelines. This individual will conduct a senior review of medical writing deliverables (CSR, IBs, Protocols, etc.), negotiate timelines, and discuss and resolve clients' comments. This role will provide written and verbal feedback to the internal team and clients when appropriate. She/he will keep abreast of current medical writing and regulatory knowledge, including Good Clinical Practice (GCP)/AMWA/EMWA along with developments and advances in clinical drug development. Join our team and help us deliver clinical trials that will improve patients' lives.   Main Job Tasks and Responsibilities: Takes a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating, and adhering to timelines, organizing document reviews, and communicating directly with the clients.Plans and organizes workload for assigned projects and tasks: identifies project needs, tracks timelines, and implements clients' requests.Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.Presents on Medical Writing processes at full-service bid defense meetings.Develops and delivers training to the global team in various aspects of medical writing.Facilitates project budgeting activities for the medical writing scope by collaborating with the BD team.Creates and maintains standard operating procedures and work instructions to prepare and maintain compliant medical writing deliverables.Oversight of a portfolio of clients.Liaison with assigned clients throughout the lifecycle of a project or program of projects to establish requirements and processes, monitor quality, and capitalize on business development opportunities.Provides scientific and technical guidance to the client and Medical Writers.Provides medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.Keeps Medical Writing senior management informed of project status and any issues that affect document quality, timelines, and adherence to contractual obligations.Serves as the primary client contact and Medical Writing representative on assigned project teams, providing support to the Project for developing efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Education and Experience:At minimum a Bachelor's degree or equivalent in medical-related field or life science. Post-graduate degree preferred.At least 10 years of experience as a clinical/regulatory Medical Writer with good clinical/scientific writing skills.Experience working on end-to-end CSR, IBs, and Protocols across different TAs is mandatory. Experience in DSUR will be considered an added advantage.An understanding of the drug development process.Broad experience managing the medical writing responsibilities associated with multiple studies at various stages.Experience in interacting with cross-functional study team members. Specific Role Requirements and Skills:Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research, and medical writing standards.Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; be attentive to details.Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within an agreed client and regulatory timelines; monitored and communicated progress against milestones; escalate complex issues appropriately.Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team membersRead, write, and speak fluent English, excellent verbal, and written communication skills.Able to assimilate and summarize large volumes of scientific data accurately, clearly, and concisely.Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Outlook.Be able to juggle multiple priorities and adapt quickly to new situations and new project demands.Culturally aware and able to work comfortably within a global team. The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected]@cromsource.com for more information.  Who will you be working for?  About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                  Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates. About TalentSource Life Sciences  TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously. CROMSOURCE is an equal opportunity employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status. Keywords: Medical Writing Director, Director of Medical Writing, Director Medical Writer, Director Medical Writing, Clinical Trials, CEP, CER, PMSR, PSUR, SOPs, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated, Clinical Evaluation Reports, medical writing, clinical study, pharmacology, clinical writing.Skills: Medical Writer, CER, CRO, Medical Writing, Outsourcing, PharmacologyLocation: United KingdomShare: LinkedIn Facebook Twitter Email

Location: Poland - Hybrid (2 days in office) Schedule: Full-time, Permanent CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Medical Writing Director.   The Medical Writing Director will function as a Lead Medical Writer for a variety of regulatory writing deliverables; and will prepare assigned documents in accordance with the internal/client SOPs and health authority requirements as per the agreed timelines. This individual will conduct a senior review of medical writing deliverables (CSR, IBs, Protocols, etc.), negotiate timelines, and discuss and resolve clients' comments. This role will provide written and verbal feedback to the internal team and clients when appropriate. She/he will keep abreast of current medical writing and regulatory knowledge, including Good Clinical Practice (GCP)/AMWA/EMWA along with developments and advances in clinical drug development. Join our team and help us deliver clinical trials that will improve patients' lives.   Main Job Tasks and Responsibilities: Takes a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating, and adhering to timelines, organizing document reviews, and communicating directly with the clients.Plans and organizes workload for assigned projects and tasks: identifies project needs, tracks timelines, and implements clients' requests.Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.Presents on Medical Writing processes at full-service bid defense meetings.Develops and delivers training to the global team in various aspects of medical writing.Facilitates project budgeting activities for the medical writing scope by collaborating with the BD team.Creates and maintains standard operating procedures and work instructions to prepare and maintain compliant medical writing deliverables.Oversight of a portfolio of clients.Liaison with assigned clients throughout the lifecycle of a project or program of projects to establish requirements and processes, monitor quality, and capitalize on business development opportunities.Provides scientific and technical guidance to the client and Medical Writers.Provides medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.Keeps Medical Writing senior management informed of project status and any issues that affect document quality, timelines, and adherence to contractual obligations.Serves as the primary client contact and Medical Writing representative on assigned project teams, providing support to the Project for developing efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Education and Experience:At minimum a Bachelor's degree or equivalent in medical-related field or life science. Post-graduate degree preferred.At least 10 years of experience as a clinical/regulatory Medical Writer with good clinical/scientific writing skills.Experience working on end-to-end CSR, IBs, and Protocols across different TAs is mandatory. Experience in DSUR will be considered an added advantage.An understanding of the drug development process.Broad experience managing the medical writing responsibilities associated with multiple studies at various stages.Experience in interacting with cross-functional study team members. Specific Role Requirements and Skills:Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research, and medical writing standards.Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; be attentive to details.Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within an agreed client and regulatory timelines; monitored and communicated progress against milestones; escalate complex issues appropriately.Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members.Read, write, and speak fluent English, excellent verbal, and written communication skills.Able to assimilate and summarize large volumes of scientific data accurately, clearly, and concisely.Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Outlook.Be able to juggle multiple priorities and adapt quickly to new situations and new project demands.Culturally aware and able to work comfortably within a global team. The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected]@cromsource.com for more information. Who will you be working for?  About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                  Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates. About TalentSource Life Sciences  TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously. CROMSOURCE is an equal opportunity employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status. Keywords: Medical Writing Director, Director of Medical Writing, Director Medical Writer, Director Medical Writing, Clinical Trials, CEP, CER, PMSR, PSUR, SOPs, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated, Clinical Evaluation Reports, medical writing, clinical study, pharmacology, clinical writingSkills: Medical Writer, CER, CRO, Medical Writing, Outsourcing, PharmacologyLocation: PolandShare: LinkedIn Facebook Twitter Email

Location: Spain - Hybrid (2 days in office) Schedule: Full-time, Permanent CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Medical Writing Director.   The Medical Writing Director will function as a Lead Medical Writer for a variety of regulatory writing deliverables; and will prepare assigned documents in accordance with the internal/client SOPs and health authority requirements as per the agreed timelines. This individual will conduct a senior review of medical writing deliverables (CSR, IBs, Protocols, etc.), negotiate timelines, and discuss and resolve clients' comments. This role will provide written and verbal feedback to the internal team and clients when appropriate. She/he will keep abreast of current medical writing and regulatory knowledge, including Good Clinical Practice (GCP)/AMWA/EMWA along with developments and advances in clinical drug development. Join our team and help us deliver clinical trials that will improve patients' lives.   Main Job Tasks and Responsibilities: Takes a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating, and adhering to timelines, organizing document reviews, and communicating directly with the clients.Plans and organizes workload for assigned projects and tasks: identifies project needs, tracks timelines, and implements clients' requests.Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.Presents on Medical Writing processes at full-service bid defense meetings.Develops and delivers training to the global team in various aspects of medical writing.Facilitates project budgeting activities for the medical writing scope by collaborating with the BD team.Creates and maintains standard operating procedures and work instructions to prepare and maintain compliant medical writing deliverables.Oversight of a portfolio of clients.Liaison with assigned clients throughout the lifecycle of a project or program of projects to establish requirements and processes, monitor quality, and capitalize on business development opportunities.Provides scientific and technical guidance to the client and Medical Writers.Provides medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copy editing and content review.Keeps Medical Writing senior management informed of project status and any issues that affect document quality, timelines, and adherence to contractual obligations.Serves as the primary client contact and Medical Writing representative on assigned project teams, providing support to the Project for developing efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Education and Experience:At minimum a Bachelor's degree or equivalent in medical-related field or life science. Post-graduate degree preferred.At least 10 years of experience as a clinical/regulatory Medical Writer with good clinical/scientific writing skills.Experience working on end-to-end CSR, IBs, and Protocols across different TAs is mandatory. Experience in DSUR will be considered an added advantage.An understanding of the drug development process.Broad experience managing the medical writing responsibilities associated with multiple studies at various stages.Experience in interacting with cross-functional study team members. Specific Role Requirements and Skills:Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research, and medical writing standards.Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; be attentive to details.Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within an agreed client and regulatory timelines; monitored and communicated progress against milestones; escalate complex issues appropriately.Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team membersRead, write, and speak fluent English, excellent verbal, and written communication skills.Able to assimilate and summarize large volumes of scientific data accurately, clearly, and concisely.Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat, and Outlook.Be able to juggle multiple priorities and adapt quickly to new situations and new project demands.Culturally aware and able to work comfortably within a global team. The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected]@cromsource.com for more information. Who will you be working for?  About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                  Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.   About TalentSource Life Sciences  TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously. CROMSOURCE is an equal opportunity employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status. Keywords: Medical Writing Director, Director of Medical Writing, Director Medical Writer, Director Medical Writing, Clinical Trials, CEP, CER, PMSR, PSUR, SOPs, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated, Clinical Evaluation Reports, medical writing, clinical study, pharmacology, clinical writing.Skills: Medical Writer, CER, clinical trials, CRO, Medical Writing, Outsourcing, PharmacologyLocation: SpainShare: LinkedIn Facebook Twitter Email

Autor/Redakteur für Bildungsinhalte - Grundschullehrer - DeutschlandStandort: Deutschland (muss in Deutschland wohnen und die Erlaubnis haben, dauerhaft in Deutschland zu arbeiten) 100% Fernarbeit von zu Hause aus. Nur in Deutschland ansässige Personen.Lohn: €14 Euro pro Stunde (Auszahlung über PayPal, monatlich) Vertrag: 12-monatiger Vertrag mit der Möglichkeit der Verlängerung. Selbstständiger Auftragnehmer, der für seine Steuern selbst verantwortlich ist. Keine Sozialleistungen. Arbeitszeiten: 20 Stunden pro WocheEinstellender Manager: Katie Pantelli-DaviesAnwerberin: Sarah Jane DalzellDas Wichtigste zuerst! Was ist Twinkl? Was ist der Zweck von Twinkl?Twinkl ist dazu da, "denen zu helfen, die unterrichten". Das ist es, was uns jeden Tag zur Arbeit bringt. Wir sind stolz darauf, Bildungsressourcen zu entwickeln, die in jeder Phase der Lernreise eines Kindes verwendet werden können.Unsere preisgekrönte Sammlung von Unterrichtsmaterialien - erstellt von Lehrern für Lehrer - bietet eine unbegrenzte Anzahl zusätzlicher digitaler und druckbarer Unterrichtsmaterialien zu einem unschlagbaren Preis. Wir haben über eine Million Materialien, und täglich kommen neue Inhalte hinzu. Sie können nicht finden, was Sie brauchen? Fragen Sie einfach! Im Rahmen unseres erstklassigen Kundendienstes erstellen wir für unsere Mitglieder maßgeschneiderte Materialien zur Unterstützung von Lehrern. Wir helfen Pädagogen und Kindern, die besten Materialien, Werkzeuge und Schulungen zu erhalten, um die Bildung in Großbritannien und auf der ganzen Welt zu verbessern.Twinkl- Materialien, die das Potenzial Ihre Kinder zum Strahlen bringen Location: Germany (must live & have permission to work in Germany on a permanent basis) 100% remote work-from-home position. German residents only.Pay Rate: €14 Euros per hour Contract: 12-month contract with an extension likely. Self-employed contractor responsible for own taxes. No benefits. Hours of work: 20 hours per weekHiring Manager: Katie Pantelli-DaviesRecruiter: Sarah Jane DalzellFirst things first! What is Twinkl? What is Twinkl’s mission?Twinkl is here to “help those who teach.” It's what brings us to work every day. We're proud to create educational resources that can be used at each step of a child's learning journey.Our award-winning resource collection - created by teachers for teachers - provides unlimited supplementary digital and printable teaching resources at an unbeatable value. We have over a million resources, and new content is added every day. Don’t see what you need? Just ask! We make bespoke resources for our members as part of our world-class customer service promise to help those who teach. We support educators and children to get the best resources, tools and training to improve the education in Germany and around the globe.You dream it, we create it for you!Die Aufgabe:Deutschland ist ein schnell wachsender Markt für Twinkl. Sie werden die kreative Freiheit haben, die Inhalte zu gestalten, die wir unseren Kunden anbieten. Unser idealer Kandidat geht über das Schreiben und Redigieren von Inhalten hinaus, indem er neue Produktideen vorschlägt, Bedürfnisse in der deutschen Lehrergemeinschaft identifiziert und seine Erfahrungen und sein Fachwissen mit anderen teilt. Es ist eine aufregende Zeit für diesen Markt. Der erfolgreiche Bewerber wird entscheidend dazu beitragen, dass diese ehrgeizigen Pläne für Deutschland Wirklichkeit werden. Es handelt sich um eine flexible Stelle, bei der Sie von zu Hause aus arbeiten können. Die Arbeitszeiten können zwischen Ihnen und Ihrem direkten Vorgesetzten vereinbart werden, so dass sie mit Ihren derzeitigen Verpflichtungen vereinbar sind.Sie werden Teil eines Teams leidenschaftlicher Pädagogen sein, die flexibel an der Erstellung und Bearbeitung von Inhalten für das neue deutsche Produkt von Twinkl arbeiten. Dieses Team erstellt eine breite Palette von Unterrichtsmaterialien für den Einsatz in der Grundschule. Dazu gehören PowerPoint-Präsentationen, Anschauungsmaterialien, Aufgabenblätter, Bewertungen und Planungen. In dieser Funktion werden Sie den Großteil Ihrer Zeit mit dem Schreiben und Bearbeiten von Inhalten für alle Altersgruppen in der Grundschule verbringen.The Role:Germany is a rapidly growing market for Twinkl. You will have the creative freedom to shape the content we offer to our customers. Our ideal candidate will be going further than writing & editing content by suggesting new product ideas, identifying needs in the German teaching community, sharing their experiences and expertise with others. It is an exciting time for this market. The successful candidate will be vital in ensuring that these ambitious plans for Germany become a reality. This is a work-from-home, flexible position, and hours can be agreed between you and your line manager to fit around your current commitments.You’ll be part of a team of passionate teaching professionals working flexibly to write & edit content for Twinkl’s emerging German product. This team creates a wide range of resources for use in Grundschule. This will include PowerPoints, display materials, activity sheets, assessments and planning. For this role, the majority of your time will be spent writing & editing content for all ages in Grundschule.Zu Ihren wöchentlichen Aktivitäten könnten gehören:Treffen mit anderen Twinkl-Teammitgliedern oder dem Country Manager, um neue Ideen zu besprechen;Schreiben von Inhalten für den deutschen Markt;Redigieren von Inhalten für den deutschen MarktEntwicklung neuer Produktideen mit dem Country Manager für Deutschland.Verfügbar für Meetings am Montag, Dienstag oder Mittwoch zwischen 10 und 14 Uhr. Your weekly activities could include:Meeting with other Twinkl team members or the Country Manager to discuss new ideas;Writing content for the German market;Editing content for the German marketDeveloping new product ideas with the Germany Country Manager.Available for meetings on Monday, Tuesday or Wednesday between 10am & 2pm. In dieser Position werden Sie:Erstellen und Anpassen von Materialien für den deutschen Grundschullehrplan und die frühen Jahre.Sie arbeiten mit anderen Content Writern und Designern zusammen, um Unterrichtsmaterialien zu erstellen.Sie erstellen neue Lehrerinhalte für unser Twinkl Deutschland Team, von der Ideenfindung bis zur Veröffentlichung auf der Website. Remote-Zusammenarbeit, enge Zusammenarbeit mit Teammitgliedern auf der ganzen Welt. (Auf Englisch)Entwickeln Sie ein größeres kommerzielles Bewusstsein, damit wir die Bedürfnisse derer, denen wir helfen wollen, verstehen können.In this role, you will:Create and adapt materials for the German Primary school curriculum and early years.Work collaboratively with other Content Writers and designers to produce educational materials.Create new teacher content for our Twinkl Germany team, from ideation stage to publication on the site. Remote collaboration, working closely with team members across the globe. (In English)Develop greater commercial awareness so we can understand the needs of those we want to help.Sie werden zusammenarbeiten mit:Katie Pantelli-Davies (Twinkl Germany Country Manager)Anderen Lehrern und Teammitgliedern - das Team besteht aus Content Writern/Redakteuren und Designern, die alle zusammenarbeiten, um Material zu erstellen und gemeinsam innovativ zu sein. You’ll work with:Katie Pantelli-Davies (Twinkl Germany Country Manager)Other teachers and team members – the team consists of Content Writers/ Editors and designers, all working together to create material and innovate together. RequirementsUm in dieser Position erfolgreich zu sein, sollten Sie:Hervorragende Kenntnisse des deutschen Lehrplans (Grundschule und frühe Jahre). Qualifikationen: Master of Education (oder gleichwertige lehrerzentrierte Qualifikationen), Staatsexamen.Mindestens 4 Jahre Unterrichtserfahrung (in den letzten 3 bis 5 Jahren) im Grundschulbereich an einer öffentlichen Schule in Deutschland.Sie haben eine Leidenschaft für das Unterrichten von Deutsch, BLB und Mathematik in einer öffentlichen Schule in Deutschland.Sie haben muttersprachliche Deutschkenntnisse. (sowohl in Wort und Schrift)Hervorragende Rechtschreibung, Zeichensetzung und Grammatikkenntnisse in Deutsch.Hervorragende Englischkenntnisse (Sie müssen in der Lage sein, sich schriftlich und mündlich zu verständigen)Kreative und proaktive Ideengeber, Texter und Redakteure. Wir sind besonders an Personen interessiert, die auch die folgenden Voraussetzungen erfüllen: Frühere Erfahrungen als Autor und Redakteur (entweder persönlich oder beruflich)Bitte beachten Sie: Wir sind nicht auf der Suche nach Englischlehrern, internationalen Schullehrern oder Kandidaten, die in den letzten 5 Jahren nicht an öffentlichen oder privaten Schulen in Deutschland gearbeitet haben. Behalten Sie aber unsere Karriereseite auf unserer Twinkl-Website im Auge, um sich über weitere Möglichkeiten zu informieren, die sich in Zukunft ergeben könnten!To succeed in the role, you will:Have an excellent understanding of the German Curriculum (Primary and early years). Qualifications: Master of Education (or equivalent teaching-centred qualifications), Staatsexamen.Have at least 4 years recent classroom experience (in the last 3-5 yrs) teaching primary levels in a Public School in Germany.Have a passion for teaching German, SU, and Math in a public school environment in Germany.Have native German language skills. (Both written and spoken)Have excellent spelling, punctuation and grammar skills in German.Have excellent English language skills (Must be able to communicate both written and spoken)Creative and proactive ideators, writers and editors. We’re are especially interested in anyone who also meets the following: Previous experience as a writer & editor (either personally or professionally) Please note: We are not looking for English teachers, international school teachers or any candidates who have not used the German Primary curriculum working in public or private schools in Germany in the last 5 years. But do keep an eye on our careers page on our Twinkl website for other opportunities that may arise in the future! BenefitsAls Gegenleistung für alles, was Sie mitbringen, bieten wir Ihnen eine spannende Aufgabe in einem schnell wachsenden und dynamischen Unternehmen mit vielen Karrieremöglichkeiten.Hier sind einige der Dinge, die Twinkl zu einem großartigen Arbeitsplatz machen:Eine freundliche, einladende und unterstützende Kultur. Wir sind der Meinung, dass Arbeit Spaß machen sollte, und wir stellen den Menschen immer über den Prozess. Flexible Arbeit von zu Hause aus.Vielfalt, Integration und Zugehörigkeit. Unser Mitarbeiternetzwerkprogramm umfasst Arbeitsgruppen für LGBTQ+, People of Colour, Behinderte (sichtbar und unsichtbar), Frauen in der Technik und berufstätige Eltern. Kontinuierliche berufliche Entwicklung (CPD). Unser sich ständig weiterentwickelndes Programm umfasst monatliche Entwicklungsgespräche, das Twinkl Management Scheme, kaufmännische Schulungen, Leadership Coaching Quads, Karrieregespräche und Mentoring. Zusammenarbeit über Kontinente hinweg! Sie werden Teil eines globalen Teams, das daran arbeitet, das Leben von Erziehern auf der ganzen Welt zu verbessern.In return for everything you can bring, we can offer you an exciting role in a fast-growing and dynamic business, with plenty of career opportunities.Here are some of the things that make Twinkl a great place to work:A friendly, welcoming, and supportive culture. We believe work should be fun, and we always put people before the process. Flexible work-from-home positions.Diversity, inclusion, and belonging. Our Employee Network Program includes working groups for LGBTQ+, People of Colour, Disabilities (visible and invisible), Women in Tech, and Working Parents. Continuous Professional Development (CPD). Our ever-evolving program includes monthly progression reviews, Twinkl’s Management Scheme, commercial awareness training, leadership coaching quads, career chats, and mentoring. Collaboration across continents! You’ll plug into a global team working to help improve the lives of educators around the world. Our Recruitment Process:HomeofficeÜber das Unternehmen:Twinkl

Autor/Redakteur für Bildungsinhalte - Grundschullehrer - DeutschlandStandort: Deutschland (muss in Deutschland wohnen und die Erlaubnis haben, dauerhaft in Deutschland zu arbeiten) 100% Fernarbeit von zu Hause aus. Nur in Deutschland ansässige Personen.Lohn: €14 Euro pro Stunde (Auszahlung über PayPal, monatlich) Vertrag: 12-monatiger Vertrag mit der Möglichkeit der Verlängerung. Selbstständiger Auftragnehmer, der für seine Steuern selbst verantwortlich ist. Keine Sozialleistungen. Arbeitszeiten: 37.5 Stunden pro WocheEinstellender Manager: Katie Pantelli-DaviesAnwerberin: Sarah Jane DalzellLocation: Germany (must live & have permission to work in Germany on a permanent basis) 100% remote work-from-home position. German residents only.Pay Rate: €14 Euros per hour Contract: 12-month contract with an extension likely. Self-employed contractor responsible for own taxes. No benefits. Hours of work: 37.5 hours per week (Full Time)Hiring Manager: Katie Pantelli-DaviesRecruiter: Sarah Jane DalzellDas Wichtigste zuerst! Was ist Twinkl? Was ist der Zweck von Twinkl?Twinkl ist dazu da, "denen zu helfen, die unterrichten". Das ist es, was uns jeden Tag zur Arbeit bringt. Wir sind stolz darauf, Bildungsressourcen zu entwickeln, die in jeder Phase der Lernreise eines Kindes verwendet werden können.Unsere preisgekrönte Sammlung von Unterrichtsmaterialien - erstellt von Lehrern für Lehrer - bietet eine unbegrenzte Anzahl zusätzlicher digitaler und druckbarer Unterrichtsmaterialien zu einem unschlagbaren Preis. Wir haben über eine Million Materialien, und täglich kommen neue Inhalte hinzu. Sie können nicht finden, was Sie brauchen? Fragen Sie einfach! Im Rahmen unseres erstklassigen Kundendienstes erstellen wir für unsere Mitglieder maßgeschneiderte Materialien zur Unterstützung von Lehrern. Wir helfen Pädagogen und Kindern, die besten Materialien, Werkzeuge und Schulungen zu erhalten, um die Bildung in Großbritannien und auf der ganzen Welt zu verbessern.Twinkl- Materialien, die das Potenzial Ihre Kinder zum Strahlen bringen First things first! What is Twinkl? What is Twinkl’s mission?Twinkl is here to “help those who teach.” It's what brings us to work every day. We're proud to create educational resources that can be used at each step of a child's learning journey.Our award-winning resource collection - created by teachers for teachers - provides unlimited supplementary digital and printable teaching resources at an unbeatable value. We have over a million resources, and new content is added every day. Don’t see what you need? Just ask! We make bespoke resources for our members as part of our world-class customer service promise to help those who teach. We support educators and children to get the best resources, tools and training to improve the education in Germany and around the globe.You dream it, we create it for you!Die Aufgabe:Deutschland ist ein schnell wachsender Markt für Twinkl. Sie werden die kreative Freiheit haben, die Inhalte zu gestalten, die wir unseren Kunden anbieten. Unser idealer Kandidat geht über das Schreiben und Redigieren von Inhalten hinaus, indem er neue Produktideen vorschlägt, Bedürfnisse in der deutschen Lehrergemeinschaft identifiziert und seine Erfahrungen und sein Fachwissen mit anderen teilt. Es ist eine aufregende Zeit für diesen Markt. Der erfolgreiche Bewerber wird entscheidend dazu beitragen, dass diese ehrgeizigen Pläne für Deutschland Wirklichkeit werden. Es handelt sich um eine flexible Stelle, bei der Sie von zu Hause aus arbeiten können. Die Arbeitszeiten können zwischen Ihnen und Ihrem direkten Vorgesetzten vereinbart werden, so dass sie mit Ihren derzeitigen Verpflichtungen vereinbar sind.Sie werden Teil eines Teams leidenschaftlicher Pädagogen sein, die flexibel an der Erstellung und Bearbeitung von Inhalten für das neue deutsche Produkt von Twinkl arbeiten. Dieses Team erstellt eine breite Palette von Unterrichtsmaterialien für den Einsatz in der Grundschule. Dazu gehören PowerPoint-Präsentationen, Anschauungsmaterialien, Aufgabenblätter, Bewertungen und Planungen. In dieser Funktion werden Sie den Großteil Ihrer Zeit mit dem Schreiben und Bearbeiten von Inhalten für alle Altersgruppen in der Grundschule verbringen.The Role:Germany is a rapidly growing market for Twinkl. You will have the creative freedom to shape the content we offer to our customers. Our ideal candidate will be going further than writing & editing content by suggesting new product ideas, identifying needs in the German teaching community, sharing their experiences and expertise with others. It is an exciting time for this market. The successful candidate will be vital in ensuring that these ambitious plans for Germany become a reality. This is a work-from-home, flexible position, and hours can be agreed between you and your line manager to fit around your current commitments.You’ll be part of a team of passionate teaching professionals working flexibly to write & edit content for Twinkl’s emerging German product. This team creates a wide range of resources for use in Grundschule. This will include PowerPoints, display materials, activity sheets, assessments and planning. For this role, the majority of your time will be spent writing & editing content for all ages in Grundschule.Zu Ihren wöchentlichen Aktivitäten könnten gehören:Treffen mit anderen Twinkl-Teammitgliedern oder dem Country Manager, um neue Ideen zu besprechen;Schreiben von Inhalten für den deutschen Markt;Redigieren von Inhalten für den deutschen MarktEntwicklung neuer Produktideen mit dem Country Manager für Deutschland.Verfügbar für Meetings am Montag, Dienstag oder Mittwoch zwischen 10 und 14 Uhr. Your weekly activities could include:Meeting with other Twinkl team members or the Country Manager to discuss new ideas;Writing content for the German market;Editing content for the German marketDeveloping new product ideas with the Germany Country Manager.Available for meetings on Monday, Tuesday or Wednesday between 10am & 2pm. In dieser Position werden Sie:Erstellen und Anpassen von Materialien für den deutschen Grundschullehrplan und die frühen Jahre.Sie arbeiten mit anderen Content Writern und Designern zusammen, um Unterrichtsmaterialien zu erstellen.Sie erstellen neue Lehrerinhalte für unser Twinkl Deutschland Team, von der Ideenfindung bis zur Veröffentlichung auf der Website. Remote-Zusammenarbeit, enge Zusammenarbeit mit Teammitgliedern auf der ganzen Welt. (Auf Englisch)Entwickeln Sie ein größeres kommerzielles Bewusstsein, damit wir die Bedürfnisse derer, denen wir helfen wollen, verstehen können.In this role, you will:Create and adapt materials for the German Primary school curriculum and early years.Work collaboratively with other Content Writers and designers to produce educational materials.Create new teacher content for our Twinkl Germany team, from ideation stage to publication on the site. Remote collaboration, working closely with team members across the globe. (In English)Develop greater commercial awareness so we can understand the needs of those we want to help.Sie werden zusammenarbeiten mit:Katie Pantelli-Davies (Twinkl Germany Country Manager)Anderen Lehrern und Teammitgliedern - das Team besteht aus Content Writern/Redakteuren und Designern, die alle zusammenarbeiten, um Material zu erstellen und gemeinsam innovativ zu sein. You’ll work with:Katie Pantelli-Davies (Twinkl Germany Country Manager)Other teachers and team members – the team consists of Content Writers/ Editors and designers, all working together to create material and innovate together. RequirementsUm in dieser Position erfolgreich zu sein, sollten Sie:Hervorragende Kenntnisse des deutschen Lehrplans (Grundschule und frühe Jahre). Qualifikationen: Master of Education (oder gleichwertige lehrerzentrierte Qualifikationen), Staatsexamen.Mindestens 4 Jahre Unterrichtserfahrung (in den letzten 3 bis 5 Jahren) im Grundschulbereich an einer öffentlichen Schule in Deutschland.Sie haben eine Leidenschaft für das Unterrichten von Deutsch, BLB und Mathematik in einer öffentlichen Schule in Deutschland.Sie haben muttersprachliche Deutschkenntnisse. (sowohl in Wort und Schrift)Hervorragende Rechtschreibung, Zeichensetzung und Grammatikkenntnisse in Deutsch.Hervorragende Englischkenntnisse (Sie müssen in der Lage sein, sich schriftlich und mündlich zu verständigen)Kreative und proaktive Ideengeber, Texter und Redakteure. Wir sind besonders an Personen interessiert, die auch die folgenden Voraussetzungen erfüllen: Frühere Erfahrungen als Autor und Redakteur (entweder persönlich oder beruflich)To succeed in the role, you will:Have an excellent understanding of the German Curriculum (Primary and early years). Qualifications: Master of Education (or equivalent teaching-centred qualifications), Staatsexamen.Have at least 4 years recent classroom experience (in the last 3-5 yrs) teaching primary levels in a Public School in Germany.Have a passion for teaching German, SU, and Math in a public school environment in Germany.Have native German language skills. (Both written and spoken)Have excellent spelling, punctuation and grammar skills in German.Have excellent English language skills (Must be able to communicate both written and spoken)Creative and proactive ideators, writers and editors. We’re are especially interested in anyone who also meets the following: Previous experience as a writer & editor (either personally or professionally) Bitte beachten Sie: Wir sind nicht auf der Suche nach Englischlehrern, internationalen Schullehrern oder Kandidaten, die in den letzten 5 Jahren nicht an öffentlichen oder privaten Schulen in Deutschland gearbeitet haben. Behalten Sie aber unsere Karriereseite auf unserer Twinkl-Website im Auge, um sich über weitere Möglichkeiten zu informieren, die sich in Zukunft ergeben könnten!Please note: We are not looking for English teachers, international school teachers or any candidates who have not used the German Primary curriculum working in public or private schools in Germany in the last 5 years. But do keep an eye on our careers page on our Twinkl website for other opportunities that may arise in the future! BenefitsAls Gegenleistung für alles, was Sie mitbringen, bieten wir Ihnen eine spannende Aufgabe in einem schnell wachsenden und dynamischen Unternehmen mit vielen Karrieremöglichkeiten.Hier sind einige der Dinge, die Twinkl zu einem großartigen Arbeitsplatz machen:Eine freundliche, einladende und unterstützende Kultur. Wir sind der Meinung, dass Arbeit Spaß machen sollte, und wir stellen den Menschen immer über den Prozess. Flexible Arbeit von zu Hause aus.Vielfalt, Integration und Zugehörigkeit. Unser Mitarbeiternetzwerkprogramm umfasst Arbeitsgruppen für LGBTQ+, People of Colour, Behinderte (sichtbar und unsichtbar), Frauen in der Technik und berufstätige Eltern. Kontinuierliche berufliche Entwicklung (CPD). Unser sich ständig weiterentwickelndes Programm umfasst monatliche Entwicklungsgespräche, das Twinkl Management Scheme, kaufmännische Schulungen, Leadership Coaching Quads, Karrieregespräche und Mentoring. Zusammenarbeit über Kontinente hinweg! Sie werden Teil eines globalen Teams, das daran arbeitet, das Leben von Erziehern auf der ganzen Welt zu verbessern.In return for everything you can bring, we can offer you an exciting role in a fast-growing and dynamic business, with plenty of career opportunities.Here are some of the things that make Twinkl a great place to work:A friendly, welcoming, and supportive culture. We believe work should be fun, and we always put people before the process. Flexible work-from-home positions.Diversity, inclusion, and belonging. Our Employee Network Program includes working groups for LGBTQ+, People of Colour, Disabilities (visible and invisible), Women in Tech, and Working Parents. Continuous Professional Development (CPD). Our ever-evolving program includes monthly progression reviews, Twinkl’s Management Scheme, commercial awareness training, leadership coaching quads, career chats, and mentoring. Collaboration across continents! You’ll plug into a global team working to help improve the lives of educators around the world. Our Recruitment Process:HomeofficeÜber das Unternehmen:Twinkl

We are currently recruiting for a full-time position of INTERNATIONAL MARKETING EXECUTIVE for our Munich based client. Its services encompass high-level content marketing solutions with magazines, websites, apps, social media channels and more as well as bespoke customer benefit strategies with a combination of events, offers and privileges created and managed exclusively for luxury business clients.TasksThe INTERNATIONAL MARKETING EXECUTIVE is a key role within the American Express Marketing Department as part of an expanding global team. Reporting to the Head of Marketing and Commercial Director, this role will work closely with the Advertising Sales team as well as the Print, Digital, Editorial and Production teams to ensure cohesive, transparent and timely communication of all revenue-driving opportunities, through considered and targeted initiatives on a global, regional and local level. The INTERNATIONAL MARKETING EXECUTIVE will be a proactive team player who helps develop and implement marketing programmes in a B2B environment and provide the Advertising Sales and Digital teams with support in the form of sales collaterals, events and pan-regional research.KEY TASKSCreate and update marketing collaterals according to brand positioning and CI guidelines as defined with the Head of Marketing, for the American Express Publications at the pan-regional, regional and local levels (incl. media kits, media site, core presentations and building blocks for sales proposals, sales sheets, brochures etc.)Obtain selected client testimonials and prepare standout case studies for integration into sales materials and B2B platformsCreate sales supporting materials for special initiatives (e.g. editorial specials, new products etc.)Coordinate, conduct and analyse primary research gathered via print and digital surveys throughout the yearAssist with the collation and analysis of third-party research and American Express brand updates to distribute to sales representative network and B2B contactsAssist with the development and execution of regular email updates to key press and advertising partners and representative networkAssist with the development and prepare strategic mailing (print & digital) as appropriateCoordinate presence and sponsorships at trade fairs and industry eventsCoordinate local market client eventsCoordinate representative training sessions (e.g. onboarding of new sales reps, annual sales conference, targeted ad hoc sales workshops)Monitor the competitive media environment and keep up-to-date with current luxury market analysisManage and liaise with external service providersAdditional support with other publications within our portfolioRequirementsHave native-level English, written and spoken (German skills would be advantageous)Ideally have minimum 2 years experience in marketing or a similar roleBe a strong copy writerHave experience with designing and conceiving collaterals, using industry standard tools such as Microsoft Powerpoint, Adobe InDesign, and Adobe PhotoshopBe creative and possess pragmatic problem-solving skillsHave a methodical and meticulous approach with excellent attention to detailBe able to work effectively and accurately under time pressureBe a strong communicatorBe able to think outside the box to come up with innovative and new ways to present our readership, products and opportunitiesBenefitsWHAT WE OFFER:Dynamic media environment with exciting projectsFlat hierarchy and an international teamDiverse range of tasks and the possibility to growAccess to on-site sport facilities at a low costPossibility of hybrid work for improved work–life balance28 days annual leaveAttractive location right on the subway with shopping opportunities in the immediate vicinityMVV-Ticket or by availability: Underground parking spaceCoffee, water, fruits/vegetablesPlease send your CV and cover letter, accompanied by your salary expectations and possible start date.Als inhabergeführte Personalberatung besetzen wir Top-Positionen auf Executive Level, im Expertenbereich sowie in der Unternehmensnachfolge — branchenübergreifend und deutschlandweit. Standort Roderer Executive Search, Munich

Our vision is to establish HUGO BOSS as the leading premium tech-driven fashion platform worldwide and to be one of the top 100 global brands. At HUGO BOSS, we work as a team to apply our knowledge, skills and experience together and create a diversity of ideas and solutions. What unites us? We love fashion, we change fashion!At HUGO BOSS, you have the opportunity to contribute your personality, ideas and creativity - because only when we break new ground together can we create something unique. Become part of our team of more than 17.000 employees worldwide and shape your future at HUGO BOSS!What you can expect: Responsible for managing the end-to-end production of seasonal assets for e-commerce platforms including marketing content (focusing but not limited to commercial content, look books and eCommerce PDP) Be the day-to-day point production contact. Collaborate closely with the in-house creative and production teams together with external production agency Ensure smooth running of daily operations to produce high quality assets within a high volume photo studio environment incl scheduling, tracking KPI's and on-time delivery Own the Ecom content production calendar. Raise awareness of upcoming briefs and keep core team updated. Lead weekly status meetings and quarterly business updates with key stakeholders Develop and lead continuous improvement of end-to-end processes including new scheduling processes and templates. Handle introduction of video for PDP and increased volume of work for wholesale partners Imbed new technologies into the team, including, use of AI in post-production, 3D product design, avatars etc Optimize asset production cycle, seek to combine shoots to find efficiencies and reduce production spend where appropriate without compromising quality. Liaise with the wider Marketing & Consumer team and key stakeholders including Creative departments, external agency partners, Merchandising & Buying teams Production coordination and logistics management - scheduling of production teams, venues and freelancers. Drive production process improvements and efficiencies Ensure pre- and post-production of assets (including final edits) are produced on brief to exceptional quality, delivered on time and on budget Budget management Ensure workflows are implemented and adhered to Collaborate across channels to ensure optimal project workflow; responsible for prioritization, resource and budget allocation, and project timelines/deadlines to ensure all projects are delivered on time. Mentor and coach team members Your profile: 7+ years of experience in an agency or in-house content production team / studio team, demonstrating cross-functional understanding and impact of creative asset development University degree in Art, Graphic Design, Business and/or relevant field of study Experience within a high volume photo studio environment for fashion brands Strong communication skills Outstanding knowledge of conflict management and negotiation Large & strong network of industry experts and partners Strong experience in managing complex projects across different channels and in a collaborative and international environment Deep knowledge of all phases and workstreams of creative asset development: briefing, concept ideation, creative, design development, planning, production and commercial Entrepreneurial and proactive mindset to drive team development Experience in the fashion/apparel industry a plus Up to 30% international and domestic travel required Fluent in English required, 2nd language a plus #LI-JW2 Your benefits: Made for Me: three days in Metzingen and two days working remotely. Our hybrid working model "Threedom of work" is as individual as your personal needs. Sustainability is one of our key values, and more than just a trend. We are committed to environmental, animal and climate protection, and human rights. Does innovation drive you? Same for us! We have digitized most of our workflows and almost fully automated our logistics centres. Exclusive discounts for shopping and arts: benefit from discounts for family and friends along with free entrance to more than 15 international art museums. High-performing people need a healthy balance. Take advantage of the employee gym, the beach volleyball field or yoga classes on the rooftop terrace. As a fashion company, we value good taste in everything - including food. Welcome to our own restaurant and café, Times. We are a global company with our employees representative of the world at large. Our inclusive culture embraces each person's authenticity and individuality. We are committed to equal employment opportunity. And we believe our equitable work environment helps unleash your full potential and inspires you to thrive.

Unsere Vision ist es, HUGO BOSS als die weltweit führende technologiegesteuerte Modeplattform im Premiumbereich zu etablieren und zu den Top 100 global führenden Marken zu gehören. Zusammen setzen wir unser Wissen, unsere Fähigkeiten und Erfahrungen bei HUGO BOSS ein und kreieren vielfältige Ideen und Lösungen. Was uns verbindet? We love Fashion, we change Fashion!Bei uns hast du die Möglichkeit, deine Persönlichkeit, Ideen und Kreativität einzubringen - denn nur, wenn wir gemeinsam neue Wege gehen, entsteht etwas Einzigartiges. Werde Teil unseres Teams aus mehr als 17.000 Mitarbeitenden weltweit und gestalte deine persönliche Zukunft bei HUGO BOSS!Zur Verstärkung unseres Teams Creative Content & Production innerhalb der Abteilung Global Corporate Communications suchen wir ab April 2024 einen Praktikanten (m/w/d) für die Dauer von sechs Monaten. Du möchtest erste Erfahrungen in globalen Kommunikationsprojekten in einem internationalen Fashion und Lifestyle Unternehmen sammeln? Dann bewirb dich und werde Teil eines dynamischen und motivierten Teams.Das erwartet dich bei uns: Übernahme von Verantwortung im Tagesgeschäft Unterstützung bei der visuellen Aufbereitung diverser Content Pieces (Bildrecherche, Bildbearbeitung, Informationsdesign, Druckdatenerstellung) Satz- und Layoutarbeiten mit den gängigen Grafikprogrammen (Adobe CC) Organisatorische Unterstützung bei Produktionen in unserem hauseigenen TV Studio Unterstützung des Teams bei der Konzeption und Umsetzung von Kommunikationsmaßahmen (Text, Video, Audio, Grafik) unserer globalen Unternehmenskommunikation Einblick in die Medien- und Öffentlichkeitsarbeit eines internationalen Konzerns Organisation von internen Events Unterstützung des gesamten Global Corporate Communications Departments und den dazugehörigen Teams Das ist dein Profil: Bachelor- (mindestens im dritten Semester) oder Masterstudium (oder bereits ein abgeschlossenes Studium) mit den Schwerpunkten Visual Design, Medien-/Grafikdesign, Kommunikations-, Medienwissenschaften oder Betriebswirtschaftslehre und/oder eine vergleichbare Ausbildung Ausgeprägtes Interesse an den Themengebieten der internen und externen Unternehmenskommunikation, wie Content Creation, Social Media, Marketing-Kommunikation und Öffentlichkeitsarbeit Organisationstalent, kommunikative Fähigkeiten und strukturierte Arbeitsweise Eigenverantwortung, Kreativität und ausgeprägte Teamfähigkeit Gute Kenntnisse in Adobe CC und MS-Office-Anwendungen Begeisterung fürs Schreiben sowie sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Das bieten wir dir: Made for Me: 3 Tage Metzingen, 2 Tage mobiles Arbeiten. Unser flexibles Arbeitsmodell "Threedom of Work" bietet dir den Freiraum, den du brauchst. Nachhaltigkeit ist für uns kein Modetrend, sondern essentiell - wir bekennen uns zu Umwelt-, Tier- & Klimaschutz und Menschenrechten. Innovation treibt dich an? Uns auch! Wir haben fast alle Workflows digitalisiert, unsere Logistikzentren funktionieren nahezu vollautomatisiert. Exklusiver Zugang zu Fashion & Art: Profitiere von Mitarbeiterrabatten, Family & Friends Days und freiem Eintritt in über 15 Kunstmuseen weltweit. Wer viel leistet, braucht einen gesunden Ausgleich: Trainiere kostenlos in unserem eigenen Gym, beim Beach Volleyball oder im Yogakurs auf der Dachterrasse. Als Modeunternehmen legen wir Wert auf guten Geschmack: das gilt auch beim Essen. Überzeuge dich selbst. Willkommen in unserem eigenen Restaurant & Café Times! Wir sind ein globales Unternehmen und unsere Mitarbeiter repräsentieren die ganze Welt. Unsere integrative Kultur respektiert und schätzt die Authentizität und Individualität jedes Einzelnen. Wir setzen uns für Chancengleichheit im Einstellungsprozess ein - und wir glauben, dass unser gleichberechtigtes Arbeitsumfeld dazu beiträgt, dein volles Potenzial zu entfalten und dich zu inspirieren, erfolgreich zu sein.

Job Description The world is changing in the way we consume products, from ownership to usership, and DigitalRoute is positioned in the centre of the transition. Because, when enterprises pivot to usage-based business models, they often make an unfortunate discovery. Their systems weren’t built to handle the massive data volumes and complexity that usage-based models generate. This causes them to leak revenue and respond too slowly to customer demand. DigitalRoute solves this by creating a real-time usage data layer for enterprises. Our products transform raw usage data into clear information for billing, in real time and at high scale.What you'll doDevelop comprehensive documentation assets such as user documentation and release documentation that meet the industry and organisational standardsObtain a deep understanding of our products and services to translate complex product information into easy-to-understand and engaging contentWork in an international company with a global marketWork as part of different teams (some remotely) as well as individuallyParticipate in the full product development cycle, from idea generation to getting feedback from end customersWe think that youLove the challenge of providing clear and concise user information for a variety of usersNative English speaker with a proficiency in UX copywriting is a plus Hava a hands-on mindset approach and you like to test a feature to create or update relevant informationAre happy to communicate with your colleagues all over the worldHave a least 2-5 years of experience in technical writingHave a passion for technology and you are eager to learn new applications and skillsHave a good attention to detailPossess excellent written and verbal communication skills in EnglishAre adept at prioritising your tasks and multi-taskingHave experience in maintaining a documentation frameworkWe also think that you enjoy having a good time with your colleagues at the local pub, going for a lunch run or joining a ski trip or why not some table tennis, chess or climbing. All work and no play is not the DigitalRoute way!We apply continuous selection, and the position may be filled before the last application date.DigitalRoute wants to be part of an inclusive and diverse environment and we are actively looking for qualified candidates irrespective of gender, sexual orientation, ethnicity, disability, or age. You will be part of a global and diverse company where our differences are our strengths.We Look forward to your application!

Highsnobiety is a brand dedicated to the latest in style, culture, and the community pushing them forward. We don't just report on what's happening - we are shaping it. From industry deep dives to product curations to our very own in-house garments, our goal is to bring you not anything and everything, but only the best of the best on all fronts. And we want you to be a part of that!We are looking for a Product Curation Intern to join our Affiliate Shopping team in Berlin!YOUR MISSION Selecting product inclusions for both paid and organic shopping focused articles Be a point of contact with clients for product approval Collaborating with the Shopping Team (Writer, Editor, Curator, Sales) to ensure that selections are delivered and executed on-time Work closely with the team to improve workflows and processes Assist Editor in SEO Strategy Assist wider editorial team with Affiliate strategy and ensure organic content is optimized from an affiliate perspective Optimize Affiliate Revenue Assist Editor in data analysis to make informed decisions on organic and paid story ideas YOUR SKILLS Students majoring in marketing, fashion or a similar field is an advantage Knowledge of current social media technologies and platforms Knowledge in current fashion and culture trends and ability to research upcoming trends Hands-on mentality and ability to get things done Able to communicate effectively in a fast-paced environment Fluency in English Experience with Excel, Google Analytics and data is a plus as well as any photo editing experience WHAT WE OFFER A bright and spacious design office, which reflects our brand and focuses on employee well-being and sustainability, located close to U Kurfüstenstrasse The opportunity to shape the company and help build a global brand in a motivating, international and diverse work atmosphere High degree of responsibility, creativity, originality, independence and creative autonomy We are constantly prioritizing attention on DEIB with internal trainings, workshops, parent friendly policies and our Employee Resource Groups (HighPower, HighPride, HighDreams & HighCulture) 2 extra days off globally for all employees on International Women's Day and Juneteenth Flexible hybrid working policy, dog friendly office, and remote international working option Attractive employee benefits (e.g. discounts in our online shop, ClassPass, access to mental health support platform Calm) We're looking forward to hearing from you!!Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. Highsnobiety is a global community of independent-minded creatives & professionals: Every perspective matters. That's why we're proud to be an equal opportunity employer. We do not discriminate on the basis of race, color, ethnicity, religion, sex, national origin, sexual orientation, age, citizenship status, marital status, disability, gender identity, gender expression, or genetic information. So if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyways.