Überblick über die Statistik des Gehaltsniveaus für "Project Administrator in Deutschland"

Location: Poland- Home based        Schedule: Freelance, Various FTEs                                    CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager II, to join their clinical operations team in Poland. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                      As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] 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. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities 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: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: PolandShare: LinkedIn Facebook Twitter Email

Location: Germany- Home based        Schedule: Freelance, Various FTEs                                  CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager II, to join their clinical operations team in Germany. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                      As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] 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. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities 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: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: GermanyShare: LinkedIn Facebook Twitter Email

Location: Spain - Home based          Schedule: Freelance, Various FTEs                                      CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager II, to join their clinical operations team in Spain. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                          As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                    Join our team and help us deliver clinical trials that will improve patients' lives.            Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process     Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.            If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] 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. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.          CROMSOURCE is an equal opportunities 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: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: SpainShare: LinkedIn Facebook Twitter Email

Location: Germany- Home based        Schedule: Freelance, Various FTEs                                     CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Senior Clinical Project Manager,  You will be working on projects from our varied client base, ranging from small to mid-sized pharma, biotech, and medical device companies.       As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                         Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with the Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDelivering  project specific trainingsOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager,  and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with and enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ www.cromsource.com/careers/job-vacancies please contact [email protected] 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. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities 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: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation                         Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, Project Management, Study ManagementLocation: GermanyShare: LinkedIn Facebook Twitter Email

Location: Netherlands - Home based  Schedule: Permanent, Full-time                       Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their internal team in Netherlands. This role is a full-time permanent opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                                 As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines and other applicable regulations.                         Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projects.Manage all project specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members.Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the clinical projects assigned.Knowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areas.Assure the proper timelines of the assigned projects.Manage the budget for the project.Monitor the workload and the performance of the project team.Plan and monitor the tasks of the team in the specific areas.Coordinate the Clinical Research Associates and Clinical Monitors activity.Collaborate with he Clinical Trial Administrators and Clinical Research Associates in terms of local authorities approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activities.Assist the Medical Monitor in preparing protocols, Case Report Forms and final Clinical Study ReportsDeliver project specific trainings.Organise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetings.Provide project updates to the Sponsor, Senior Project Manager and Project Director/Leader as required.Inform the Project Director/Leader about any issues.Perform co-monitoring visits for the assigned clinical projects as necessary.Act as a tutor for Project Coordinators and Project Manager IMaintain relationships with the Sponsor, including providing project updates.Prepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying and enforcing Company procedures. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similar.Excellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Benefits of Working in Netherlands:Competitive SalaryGroup health insuranceGreat pension scheme24 vacation daysInternet reimbursementCompany Car with fuel card depending on the function.Dedicated Line Manager The Application Process         Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step. If you would like to discuss the role before applying through the website @

Location: Belgium - Home based    Schedule: Permanent, Full-time                           Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their internal team in Belgium. This role is a full-time permanent opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                                  As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines and other applicable regulations.                             Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projects.Manage all project specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members.Keep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assigned.Knowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areas.Assure the proper timelines of the assigned projects.Manage the budget for the project.Monitor the workload and the performance of the project team.Plan and monitor the tasks of the team in the specific areas.Coordinate the Clinical Research Associates and Clinical Monitors activity.Collaborate with he Clinical Trial Administrators and Clinical Research Associates in terms of local authorities approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activities.Assist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project specific trainings.Organise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetings.Provide project updates to the Sponsor, Senior Project Manager and Project Director/Leader as required.Inform the Project Director/Leader about any issues.Perform co-monitoring visits for the assigned clinical projects as necessary.Act as a tutor for Project Coordinators and Project Manager IMaintain relationships with the Sponsor, including providing project updates.Prepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying and enforcing Company procedures. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similar.Excellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Benefits of Working in Belgium:Competitive SalaryGroup and hospitalisation insuranceElectronic meal vouchersInternet reimbursement The Application Process           Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step.                        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please send an mail to: [email protected] for more information.                     Who will you be working for?                                            About CROMSOURCE                           CROMSOURCE is a family owned international, full-service Contract Research Organisation who, 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 on 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 to 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.                                                         CROMSOURCE is an equal opportunities 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: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research OrganisationSkills: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Senior Clinical Project Manager, clinical trials, CRO, Medical Devices, Study ManagementLocation: BelgiumShare: LinkedIn Facebook Twitter Email

System Administrator IT Support (m/f/d) - 436-11403 Competent, personal and proactive - that's top itservices AG. We provide companies with comprehensive advice on their IT projects and support them with the professional placement of specialists and managers. For permanent positions, projects or on a temporary basis. Are you looking for your next challenge? Then we are looking for you! Together we want to create significant added value both for your individual development and for the success of our clients! Take up the challenge and fill a vacant position at a leading information technology company as System Administrator IT Support (m/f/d). Job Description Ensuring the operation of servers and the network infrastructure Installing and configuring hardware and software and carrying out updates Installing software on mobile devices and configuring telephone systems Responsibility for error analysis and troubleshooting Your qualification Completed training or studies in the IT sector or a comparable qualification Professional experience as a system administrator and in IT support as well as in the operation of servers Know-how in the implementation of security measures, in infrastructures and with hardware and software Business fluent in written and spoken German Information about the project Transparent and fast application process with a binding response within 14 days Trustworthy & personal support at all times - partnership is the basis of our cooperation Networking with interesting and renowned companies Apply Do you recognize yourself? Then send your documents to [email protected] quoting the reference number 436-11403. Iryna Becker will be happy to answer your initial information requests and questions by telephone on +49 231 565569-80. We look forward to hearing from you soon! Apply directly at https://www.top-itservices.com/11vf6kk You can also find other interesting vacancies on our homepage: https://www.top-itservices.com/annoncen If no explicit differentiation is made in the text between the female, male and other forms for the sake of better readability, all are always meant.

Assistant to Head of Spare Parts / Project Administrator (m/f/d) Job code The KMS Group is a service company in the field of Human Resources. Our portfolio includes temporary staffing, recruitment, outsourcing and onboarding. site management in the fields of aviation, vehicle construction, mechanical engineering, steel construction, warehousing/logistics, finance/office and engineering. We offer you an innovative and challenging workplace, an attractive salary and good development opportunities. We are looking for you as an enthusiastic and reliable employee (m/f/d) for one of our customers in the field of: Mechanical Engineering at the Augsburg site, for a committed and motivated personality to join the team at the earliest possible date. Your tasks Supporting the Head of Spare Parts in all organizational and administrative matters Organization of meetings, workshops and business trips (including travel expense accounting) Creation of evaluations, status reports and professional presentations Creation and monitoring of customer contracts Independent implementation of projects Collaboration on special projects for the specialist area Your qualifications Completed commercial or business management training Several years of professional experience in the assistance and project area Experienced handling of MS Office Solution-oriented and independent way of working Good written and spoken English skills High level of reliability and trustworthiness Strong communication and teamwork skills, high level of discretion We offer An exciting challenge in a dynamic, internationally successful company a permanent position with us and, if you perform very well, the chance of being taken on by our client Very good pay in line with performance Up to 30 days vacation depending on length of service Company pension scheme Development and training opportunities on/off the job HAVE WE PIQUED YOUR INTEREST? Then we should definitely get to know each other! Start a career for your future with us. Apply now( https://kmszeitarbeit3.hr4you.org/job/apply/9372?page_langde ) KMS Zeitarbeit GmbH Niklas Baltrusch Niklas Baltrusch Augsburg branch Zimmererstrasse 20 86153 Augsburg 0821 45 44 37 - 18 [email protected]

Die Calderys Gruppe ist ein weltweit führender Anbieter für Industrien, die unter Hochtemperaturu00adbedinu00adgunu00adgen arbeiten. Calderys ist auf den Wärmeschutz von Industrieanlagen spezialisiert und bietet eine breite Palette an feuerfesten Produkten und fortschrittlichen Lösungen zur Verbesserung von Stahlguss, metallurgischen Flussmitteln und Formgebungsu00adverfahren. Als internationales Unteru00adnehmen bieten wir unseren mehr als 6.500 Mitarbeitern an unseren verschiedenen Standorten auf über 5 Kontinenten eine Welt voller Möglichkeiten.Wir setzen unser über 150-jähriges Know-how ein, um eine positiveu00adu00adu00ad Wirkung für unsere Stakeholder zu erzielen. Jeden Tag arbeiten wir an einer nachhaltigen Zukunft durch Teamarbeit, Kundenu00adorientierung und eine proaktive Denkweise. Wir sind ein Unternehmen, in dem Leistung anerkannt und Lernen gefördert wird; ein Umfeld, in dem Sie wachsen und Ihr Potential entfalten können. Ein Arbeitsplatz, an dem jeder Tag ein neuer Tag ist und an dem es niemals langweilig wird. Project Service Administrator - Projektsachbearbeiter (m/w/d) Neuwied, Rheinland-Pfalz, Germany Mission:Für unser Projektteam in Neuwied suchen wir Sie als Project Service Administrator, um unsere Montageprojekte abzuwickeln. In dieser Rolle sind Sie u.a. für die Erstellung von Angeboten in SAP, die Bearbeitung von Kundenbestellungen mit dem Projektleiter sowie die Versandabwicklung zuständig. Verantwortlichkeiten:Erstellen von Angeboten in SAPBearbeitung von Kundenbestellungen in Zusammenarbeit mit der Projektleitung (Einholen von Lieferantenerklärungen, Montagebestellung von Subunternehmen, Versandabwicklung etc.)Unterstützung des Controllings beim Monats- und JahresabschlussUnterstützung der Projektleiter bei der Abwicklung von Montageprojekten (Dokumentation, Zuarbeit in der Qualitätssicherung, Rechnungsstellung, Koordination verschiedener Schnittstellen etc.) AnforderungenAbgeschlossene kaufmännische AusbildungMin. 3 Jahre Erfahrung in der administrativen Abwicklung von ProjektenErfahrung mit Google Workspace, MS Office 365, SAP (R3)Gute Deutsch- und Englischkenntnisse notwendigGute Kommunikationsfähigkeiten Ihre VorteileArbeitgeberfinanzierte betriebliche AltersvorsorgeVermögenswirksame LeistungenGruppenunfallversicherungHybrides Arbeiten30 Tage UrlaubGute Erreichbarkeit und kostenlose ParkplätzeCorporate Benefits Ihr KontaktJETZT ONLINE BEWERBENWeitere Informationen darüber, was uns ausmacht, finden Sie auf calderys.com.

IT-Project Manager (all genders) Schwerpunkt CRM Vollzeit | Services | Augsburg Über unsDie baramundi software GmbH ist ein dynamischer Spezialist für IT- und OT-Lösungen. Seit Gründung im Jahr 2000 entwickeln und vertreiben wir innovative Endpoint-Management-Software und -Services Made in Germany. Kernprodukt ist die u201ebaramundi Management Suiteu201c. Aktuell verwalten Administrator:innen in mittelständischen Unternehmen und Organisationen weltweit damit ca. 3 Millionen Endpoints sicher und effizient. Über 290 Mitarbeitende in Deutschland, Großbritannien, u00d6sterreich, Schweiz, Polen, Italien und den USA engagieren sich dafür, die baramundi Management Suite mit Leidenschaft zu entwickeln, zu vertreiben und unsere Kunden mit umfangreichem Service zu unterstützen. Wir freuen uns, dich kennenzulernen! Willkommen bei baramundi! u201eGib unseren Projekten deine Handschrift.u201cEine der wichtigsten Konstanten bei baramundi? Abwechslung. Ob Sales, Marketing, Finance, Support, Services oder Entwicklung: Unsere Abteilungen sind dein Fachbereich. Genau wie das Entwickeln, Managen und Optimieren von Projekten. Deine Expertise macht Abläufe rund und Projekte erfolgreich. Der dynamische baramundi Spirit in unserem PMO & BA Team hilft dir dabei. So wird aus Daily Work Teamwork. Und daraus der perfekte Workflow. Tu, was du am besten kannst:PLANEN Du verantwortest die Planung und Steuerung unterschiedlichster interner IT-Projekte und stellst den Projekterfolg unter Einhaltung der vereinbarten Termin-, Budget- und Qualitäts-Zielen sicherINNOVATIV DENKEN Du bist maßgeblich daran beteiligt, unsere Business Applikationen Schwerpunkt CRM und Sales-Prozesse innovativ weiterzuentwickeln und zu digitalisierenETWAS BEWEGEN Du unterstützt aktiv die Projektumsetzung und treibst diese voranBERATEN & BEGLEITEN Enge Beratung und Abstimmung mit den beteiligten Fachbereichen sowie das Management von externen Dienstleistern und Softwarelieferanten AUSTAUSCH PFLEGEN Du kommunizierst und koordinierst zwischen allen Stakeholdern und präsentierst Projektergebnisse souverän auf Management EbeneVORAUSSCHAUEN Die Mitwirkung bei der Projektportfolio- und Budgetplanung sowie bei der Weiterentwicklung von internen Projektmanagement- Methoden und -Standards runden Deine Aufgaben abSPASS HABEN Du findest deinen Platz in unserem bunten und kollegialen Umfeld Bring mit, was wir an dir schätzen:Abgeschlossenes Studium der Informatik, (Wirtschafts-)Informatik oder BWL, alternativ eine vergleichbare Ausbildung mit Berufspraxis Mehrjährige Berufserfahrung in der Leitung von Projekten sowie sicherer Umgang mit klassischen und agilen ProjektmethodenGrundlegende Kenntnisse von ERP- und CRM-Systemen Unternehmerisches Denken und Handeln sowie informationstechnisches VerständnisSpaß an komplexen Themen und eine ausgeprägte Hands-On und ServiceorientierungKommunikations-, Präsentations- und ModerationskompetenzSehr gute Deutsch- und Englischkenntnisse runden dein Profil ab So ticken wir! 10 Gründe für deinen Einstieg bei baramundi!#1 KOMM' IN RUHE AN Unser Rundum-Sorglos-Paket macht den Einstieg besonders leicht. Deine persönliche:r Startbegleiter:in zeigt dir alles: vom Welcome-Frühstück bis zum vollausgestatteten Arbeitsplatz. #2 FÜHL DICH ZUHAUSE Das Mittagessen im hauseigenen Restaurant baraGusto und viele leckere Kaffeevariationen im gemütlichen Cafu00e9Mundi gibt es kostenlos. Wir kümmern uns um deine Post und Pakete. Einmal im Monat treffen sich alle baramundianer während der Arbeitszeit zum Pizzaessen und Quatschen. Einfach so. #3 ERFAHRE WERT UND WERTSCHu00c4TZUNG Wir glauben an Werte und leben sie: Miteinander und Vertrauen. Mut, Begeisterung und Kompetenz. Unsere Kommunikations-Kultur ist offen und ehrlich. Genau wie die regelmäßigen Team-Feedbacks. #4 LASS DICH BELOHNEN Unsere Anerkennung spürst du auch. Erfolgs-Boni ist ebenso selbstverständlich wie Weihnachtsgeld, betriebliche Altersvorsorge und Teamevents. #5 GENIESSE DAS LEBEN Arbeitszeit ist Lebenszeit. Deshalb darfst du sie bei uns individuell gestalten. Mit Gleitzeit in Voll- oder Teilzeit, Home-Office, Mobile Work und sogar Sabbatical-Option. Bei einer 37 Stunden Wochenarbeitszeit mit 30 Tagen Urlaub. #6 BLEIB GESUND Wir wollen, dass es dir gut geht. Deshalb haben wir ergonomische Möbel und organisieren Gesundheitstage, Massagen, Yoga- und Laufgruppen. #7 ENTWICKLE DICH WEITER Dein persönliches und fachliches Weiterkommen ist uns wichtig. Wir bezahlen Fortbildungen, Sprachkurse und Coachings während der Arbeitszeit. Sogar 2-jährige Arbeitsaufenthalte in unserer Niederlassung in den USA sind drin. #8 ARBEITE AUF AUGENHu00d6HE Wir sind alle per du, vom Azubi bis zur Geschäftsführung. Komplizierte Hierarchien gibt es bei uns nicht. #9 DEINE FAMILIE IST UNS WICHTIG Familie bedeutet bei uns da sein, sich kümmern und gegenseitig unterstützen. Das tun wir mit Kita-Zuschüssen und Ferienbetreuung genauso wie bei unserem Familien-Sommerfest. #10 MACH UNS NOCH BESSER Wir wollen ein großartiger Ort und Arbeitgeber sein. Dazu brauchen wir ehrliches Feedback. Du hast Anregungen und Ideen, die uns noch besser und glücklicher machen? Wir setzen sie um. Kontaktiere uns! Kontaktiere uns!Deine persönliches Recruiting-Team Giulia Di Chiazza, Alexandra Wagner, Doris Hoefflinger +49 821 5 67 08 - 150 Jetzt bewerben Jetzt bewerben

We have an interesting opportunity for an IT System Administrator (m/f/d) with our well-known customer in the precision engineering sector. Our customer in Dresden specializes in tailor-made infrastructure, services and secure supply chain solutions. Our task as DIS AG is to bring you and our client companies together. Our individual advice and placement is free of charge for you! The position as IT Administrator (m/f/d) is to be filled in direct recruitment. This position is to be filled within the framework of direct placement / within the framework of personnel placement. IT System Administrator (m/f/d) in Dresden Your tasks: Working closely with specialist departments, advising and training managers and employees Processing inquiries and faults in 1st and 2nd level support Responsibility for IT administration, authorization management and implementation of new IT components Responsibility for network, internet and further development of network security Management of suppliers and service providers Realization of projects for the introduction, further development and replacement of IT systems Co-design of IT service processes in cooperation with the IT team at the locations in Baden-Wu00fcrttenberg and Thuringia Your qualifications: Completed training as an IT specialist for system integration or studies in the field of (business) informatics Knowledge of IT security, IT project and service management, network and back-up systems First experience in IT system administration in a manufacturing company High degree of self-motivation, teamwork, independent way of working Process, solution and goal orientation including quick comprehension skills At least a C1 level of German Permanent employment contract Attractive salary and profit-sharing as well as special payments Flexible working with flexitime and home office as well as 30 days' vacation Further training opportunities Job bike / job ticket With us, your career path will become your personal walk of fame - we offer you exciting prospects in the areas of assistance & secretarial services, marketing, sales, HR and purchasing & logistics. Click on \"Apply directly\" now!

Do you have a good understanding of IT systems and processes? Are you also ready for a new professional challenge? Then you've come to the right place! Our innovative client company in the medical technology sector is looking to strengthen its IT infrastructure team as soon as possible. The position is to be filled in Offenburg and as part of direct recruitment. This position is to be filled within the framework of direct placement / within the framework of personnel placement. System administrator (m/f/d) in medical technology - ID: 245589.2 Your tasks: Your main tasks will include the administration and optimization of IT systems. You will be responsible for supporting and managing the server and network landscape. In addition to the project planning and implementation of system integrations, you will be involved in the design and expansion of the IT infrastructure. You will also support your colleagues with technical questions and problems. Participation in various IT projects rounds off your field of activity. Your qualifications: You have successfully completed your training or studies in the field of computer science You also have initial professional experience in the above-mentioned field. You are already familiar with network technologies, firewall, routing, VLAN etc. as well as VM-Ware. You are also familiar with Microsoft-based operating systems and server applications. You also have knowledge of Exchange as well as backup and archiving systems. You also have a very good command of German and English. Personally, you impress with your IT affinity and flexibility as well as your service orientation and ability to work in a team. Very quick feedback on your application Open exchange via telephone, digitally or in person Career prospects beyond the current job offer Preparation, briefing, coaching for job interviews with our clients Appreciative and trusting support The master plan for your career: We will find exactly the job that suits you. Click on \"Apply directly\" now!

ESRA GmbH is a regionally successful company in the field of security technology. The planning, installation and maintenance of burglar and fire alarm systems as well as video security systems are just as much a part of our work as the installation and support of data networks and telephone systems. For our headquarters in Reichenbach or Chemnitz, we are looking for the next possible date for a IT System Administrator (m/f/d) part-time or full-time **** Your tasks: System/IT administrator in the area of Windows/Microsoft 365 and IP security (firewall admin, Kaspersky, Yubikey, 2FA, data backup management, etc.) in presence and remotely Management of Synology NAS and other storage systems (IP video recorder) Support of our ERP program ESoffice (current) and future ones Participation in customer projects in related subject areas Project planning and project management of IT, IP video and telecommunications projects conceivable Supporting our technicians with programming and commissioning on various systems **** Your profile: Completed vocational training in the field of computer science, completed IT studies or career changer with relevant professional experience At least two years of professional experience is desirable Very good technical understanding Openness to new systems and willingness to continuously expand knowledge Independent, structured and solution-oriented approach Class B car driver's license We offer: Pleasant working atmosphere in a motivated, open & cooperative team Compatibility of family and career Permanent employment contract in a constantly growing company Workplace with modern technology Provision of iPad, smartphone and company car Regular training and further education opportunities Free drinks and muesli bar Shopping discounts and prevention measures If you are looking for a modern workplace in a family-friendly company, then apply now with your complete application documents and the earliest possible starting date by e-mail to bewerbung (https://mailto: [email protected] ) @ esra.de or by post to ESRA GmbH, Friedensstrau00dfe 64, 08468 Reichenbach. You can reach us by telephone on 03765 78900 Your contact person is Simon Strobel. We look forward to hearing from you!

Join us and write your success story with us! For over 25 years, meco has been offering its customers IT solutions from a single source - from strategy consulting to day-to-day business management. With a wealth of experience, expertise and great passion, we work internationally for customers from various industries. They rely on us because we take a holistic, strategic approach and act pragmatically. Our motto is: meco makes it easy! It's easy - become part of the meco team! At the earliest possible date, we are looking for you for our location in Weingarten as: IT System Administrator with focus on VMware & Veeam (m/f/d) Simply exciting Exciting and varied tasks await you: Handling business trips and training courses Design, implementation and further development of virtualization solutions based on VMware & Veeam System management of virtualized infrastructures Development and implementation of storage and backup concepts Implementation of customer projects in the VMware and Veeam environment Virtualization/ Cloud Storage, SAN network Backup Monitoring Server/client systems Consulting, planning and implementation Creation of project and concept documents Service/maintenance of systems Documentation Support Technical project management/project responsibility in coordination with the team leader Traveling, installations at the customer's site Simply join in To join our team, you need the following: Completed IT training, e.g. as an IT specialist in system integration Initial experience with VMware components desirable, we will develop everything else together Independent way of working as well as high service orientation and commitment Continuous further development is important to you Good German and English skills round off your profile You are characterized by commitment and reliability Simply feel good So that you feel comfortable with us, we offer you: A secure job in a collegial working environment Reliable and flexible working time model 30 days vacation + special leave Performance-related pay Responsible tasks in a family-run company in the region Variety, new challenges and responsibility Short communication channels thanks to a flat and familiar company structure Individual development and training opportunities Mobile working Capital-forming benefits & company pension scheme Free coffee and tea variations, as well as soft drinks and water dispenser Bicycle leasing, corporate benefits, loyalty bonuses, employee events Do you not have all of these skills or are you a career changer? No problem, let's talk! Simply apply Join us and send us your application. We look forward to getting to know you soon. meco IT GmbH Liebfrauenstrau00dfe 8 88250 Weingarten | Phone +49 751 79132 174 | [email protected]

IT System Administrator (m/f/d) We, Mitchells & Butlers Germany GmbH, are a leading and sustainably growing system catering company with currently 43 locations throughout Germany. We are looking forward to strengthening our IT team at our head office in Wiesbaden with immediate effect or by arrangement. The IT department, partly with the involvement of external service providers, provides our locations with significant support in the areas of telephony, the cash register system and the entire PC, server and network infrastructure, both on the hardware and software side. Among other things, the department uses a ticket system for this purpose. This is how you can imagine your new job: You will accompany and support us in new document management projects, monitoring the systems used and signing and releasing internal documents In addition, we would like you, after your detailed training, to take project responsibility and independently monitor the setup and monitoring of all systems at our head office and locations You will also support us in replacing the server hardware in the locations and upgrading the W-LAN infrastructure Together we go into the planning and implementation of Microsoft Azure and Microsoft Office 365 projects You will also take care of user documentation and training You accompany and support us in the certification according to ISO 27001 We are currently working as a team on the following IT projects: Customization of Devolution Remote Desktop Manager with data and access to all locations for IT support Distribution and customization of CI signature Customization of the Sophos firewall for all locations As you describe yourself: At best, you have already worked as an IT system administrator or network administrator for three to five years. You also have experience in the following areas: MS client and server experience, especially WIN10, WIN11 - Server from 2012R2 If possible, knowledge of Azure AD MS Exchange from version 2013 Microsoft Office 365 and MS SharePoint We look forward to any further experience of the skills listed below. However, they are not essential: AD design and/or GPO design MS-SQL experience Linux Project and quality management Inventory and documentation (Docusnap) Sophos Firewall Hypersoft POS system And this is what you can expect from us: Many attractive additional financial benefits, such as a performance-related bonus system or a voluntary Christmas bonus, which we will be happy to explain to you in more detail in a personal meeting In addition to the contractually agreed annual leave, we grant you 7.5 vacation days (pro rata) A monthly inflation adjustment bonus of 100.00 euros net until 31.12.2024 Pluxee meal vouchers in the amount of u20ac7.20 per working day, which we offer in retail stores and selected restaurants can redeem Additional company health insurance from the sixth month of employment A permanent, full-time contract offers you planning security Trust-based working hours and the option to work from home ensure a better work-life balance between family, career and private interests. During induction, presence at the head office is necessary; after successful induction, 2 home office days per week are possible. Through intensive induction, as well as external and internal training opportunities, the chance to develop further with us Of course, we will equip you with the appropriate technology such as a laptop and smartphone Send us your documents by e-mail, stating your possible starting date and your desired salary. Do you have any questions about this vacancy? Then just give us a call!

Administrator:in IT Infrastructure - Server Systems m/f/d With its care network of hospitals, medical care centers, prevention, early detection and rehabilitation services as well as residential and nursing care services for senior citizens, Contilia accompanies people in the central Ruhr area throughout their lives. Under the symbol of the lime tree, more than 7,000 employees form a reliable and innovative community that is committed to maintaining health, overcoming illness and ensuring the best possible quality of life. In addition, we support people in shaping phases of their lives that require assistance in a self-determined way and in managing their everyday lives as independently as possible. Contilia.Digital provides all IT services for the Contilia Group and its facilities. Strategically and operationally, we design the application and infrastructure landscape centrally in the project, operation and service stages for the approximately 7,500 users. We use enterprise components, solutions and services from renowned manufacturers and suppliers. Our experts implement interoperable processes and architectures with a focus on performance, stability and security. For the Infrastructure Operations team, we are looking for a:n dedicated:n Administrator:in IT Infrastructure (m/f/d) server systems Tender number: 13266 Your tasks Administration, installation, operation, maintenance and performance tuning of server systems Windows, MS SQL, DFS, Exchange Citrix, VMWare Backup, monitoring, security solutions Ensuring and continuously improving stability, security and performance Development of new concepts, as well as analysis and further development of the existing infrastructure Diagnosis and troubleshooting of the various server systems Joint implementation of IT infrastructure projects with internal and external teams Coordination of manufacturers and service partners in the event of faults / troubleshooting (3rd level) Creation of system and application documentation Completed training in the field of IT Several years of professional experience and proven knowledge in system administration Very good knowledge in the areas of Windows Server, Database, Storage, Mail, Virtualization, Backup, Security Very good comprehension skills and the ability to analyze complex contexts independently Clear communication skills and an open and courteous manner characterize you You have a structured and independent way of working and take a solution-oriented approach to problems The ability to work in a team and a strong service orientation round off your profile Exciting projects The opportunity to get involved An attractive salary in accordance with AVR-Caritas including an annual special allowance A company pension financed by the employer at 5.6% of gross salary with the Kirchliche Zusatzversorgungskasse Köln (KZVK) Option of a discounted company ticket with Ruhrbahn Welcome event for our new employees Wide range of employee benefits and discounts (e.g. corporate benefits) Flexible participation in mandatory training courses through our e-learning program Numerous offers in our internal health management program Regular training and further education Curious? If you have any questions, please call Lars Jakubowski, Head of Infrastructure, Operations & Services, on +49 201 65056-4532. We look forward to hearing from you!

IT Project Management / IT Administrator (m/f/d) Your tasks: Management, planning, control and documentation of IT projects and programs of various sizes and complexity as well as carrying out the necessary activities across all project phases for our customers Administration and further development of our customers' servers, networks and cloud services Ensuring the security, availability and performance of IT systems Analyzing and rectifying technical faults and errors Advising our customers on the selection, implementation and customization of IT solutions Creation of technical documentation and training materials Responsibility for adhering to the set budget and time limits as well as the promised quality for IT projects and IT parts of business projects Efficient and target group-oriented communication between internal and external project participants You have... a completed apprenticeship or degree in the IT sector or a comparable qualification Several years of professional experience as a system administrator or consultant Knowledge of modern network and system infrastructures Knowledge of Windows Server, Azure and Microsoft 365 Knowledge of operating environments and operating software of modern IT devices and IT systems Enjoy putting the customer at the center and tackling their challenges Ideally basic knowledge of project management Very good knowledge of German and passable knowledge of English a strong communicator with a goal-oriented personality who can inspire and inspire others with their manner a pragmatic and solution-oriented way of working with a hands-on mentality to get things moving and move things forward We offer you... Individual coaching for your development A thorough induction with a mentor Flexible mobile options for a good work-life balance Further training and career opportunities according to your talent and motivation Modern IT equipment (notebook, smartphone for private use) An attractive salary that recognizes your work Joint company activities for more fun and team spirit a weekly sports program with a trainer for your fitness and health A strong team with friendly colleagues who support and inspire you value-oriented cooperation based on the jointly developed mission statement the chance to make a real difference with exciting and innovative projects About usWe turn business processes into a positive IT experience. 100% service quality as the measure of all things is our mission. We are a medium-sized, owner-managed company based in Babenhausen (Hesse). We have been operating successfully on the market in the Rhine-Main region and in the Frankfurt am Main area, throughout Germany and Europe, since 1988. In the process, we have built up a high level of experience and expertise in IT. For us, the most important thing is to understand how our customers work in order to determine their needs in the best possible way and to support companies with precisely tailored hardware and software. We offer suitable solutions for SMEs in the areas of cloud, infrastructure, digitalization and security.

Job Description Are you a detail-oriented individual with a keen interest in data management and a strong system understanding? We are currently offering an opportunity to play a pivotal role at Swedish Match, ensuring the accuracy and completeness of product data for new and existing products.About the positionSwedish Match is expanding its business and product range, and with our global expansion, we need to further increase our team. We are now seeking a Master Data Administrator for the Masterdata department. This department is part of the Product Management function within the Innovation Center unit, which operates at the interface between development and production. It focuses on products in the categories of snus, nicotine pouches, and tobacco- and nicotine-free portion products. The team is based at the development center in the Göteborg factory and collaborates closely with the factories in Göteborg and Kungälv, Silkeborg in Denmark, and Roma on Gotland.As a Master Data Administrator, you will be crucial in ensuring the accuracy and completeness of product data for Swedish Match’s new launches and existing products. Your responsibilities will include coordinating data collection, reviewing and validating information, and supporting project management to maintain the timeline for product deliveries. This role is essential in ensuring that the company’s products maintain high quality and comply with relevant regulations and standards, while also optimizing the manufacturing process for increased efficiency.

System administrator Linux and Windows Allgeier Public is one of the leading full-service providers for digitization projects for public administrations in Germany. Our teams of around 500 colleagues shape the digital transformation of public administration and support our customers with expertise, advice and solutions. Join Allgeier Public and develop the future of Germany with us! Become part of our team and start at Allgeier Public from September at the Munich location with remote work as System Administrator Linux and Windows (m/f/d). Your tasks Configuration and administration of Linux and Windows servers Administration of network components, switches and firewalls Supporting the team in the test lab Coordination with the customer in the area of process optimization and requirements Creation of the documentation Your profile Completed studies or completed vocational training with several years of professional experience in the IT environment Several years of practical experience in the administration of Linux and Windows systems Completed certification in Microsoft or Cisco is an advantage Good written and spoken German language skills Your advantages Mobile working: Depending on the project, mobile working is possible with us by arrangement. Family-friendly: We top up your salary to 100% if your child is ill. There is also the option to arrange an individual childcare allowance. Vacation days: 30 vacation days are a matter of course for us. Job ticket: So that you can easily reach our locations, we also support you with an allowance for the Germany ticket. Culture: We live the \"Duz\" culture, have short communication channels and are happy to help you with questions across departments. Employees refer employees: Do you know someone in your circle of friends or family who is looking for a job? Your recommendation will definitely be rewarded. Even more benefits: possibility of a company pension scheme within our attractive group contract with an employer contribution of 20%, employee discounts, gifts for personal occasions. For more information on this and other offers, please contact us at any time. In order to guarantee fast processing, please quote the reference number 149854. Additional information: Requirements for the applicant: Advanced knowledge: Network technology Cisco Expert knowledge: Windows Server 2022 operating system, firewall systems Mandatory: Linux operating system

IT administrator From product to perfect product. From the job, to the perfect job. Become part of the team at Europe's largest flexographic printing company. Since 1961, we have been penetrating the European packaging market with innovative packaging solutions, state-of-the-art machine technology and close cooperation between a team of almost 400 employees. What are you waiting for? We are looking for an IT administrator Your tasks will include: Administration, operation and further development of the client and server infrastructure 1st & 2nd level support for hardware and software Assumption of responsibility for IT projects Documentation, development of IT strategies as well as optimization and adaptation of future IT system design If you are interested, we look forward to receiving your application! Additional information: Requirements for the applicant: Basic knowledge: Project management Expert knowledge: Client-server technology, security systems (IT), data security Mandatory requirement: Microsoft Office