Überblick über die Statistik des Gehaltsniveaus für "Clinical Data Manager in Baden-Württemberg"

Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care. Job Description Primary Function of Position: The Clinical Sales Associate will help maximize the utilization of installed da Vinci Surgical Systems. Roles and Responsibilities: Implement the clinical sales plan defined by the Clinical Sales Manager to drive utilization of the da Vinci Surgical System. Become a da Vinci Surgery expert mainly across core indications for the region in order to support the development of surgical robotics programs in the assigned territory. Support regional Sales and Marketing development events that create system awareness and procedure adoption. Develop a da Vinci Surgery plan for each surgical team to insure they are capable of using the system independently within a reasonable time frame based on their volume and access to the system. Drive utilization of the da Vinci system by working with surgical teams to review and select appropriate cases and ensure consistent usage of the da Vinci. Drive continuous expansion of the user base by working with key hospital staff and surgeon thought leaders to develop a qualified lead funnel; interactions with C-level, senior hospital staff and KOL's would be supported by the Clinical Sales Manager. Lead surgical teams through training sessions, helping them understand system operations, OR integration and da Vinci Surgery applications. Be a resource to the surgical team, providing guidance and insight on the use of the da Vinci Surgical System through providing case support. Responsibly manage administrative tasks; reporting of sales/procedures, outcomes of sales activities, submission of expense reports, etc. Qualifications Required Knowledge, Skills, and Experience: Bachelor’s degree or equivalent experience required. Minimum of two years of experience in support and training in medical device industry or minimum of two years of prior sales experience in healthcare. Successful experience as sales support or successful experience in Sales. Excellent interpersonal skills and communication skills. Fluent in English and German language. Ability to travel up to 50%, dependent upon account distribution. Proven ability to work effectively as part of a team. Knowledge of the Operating Room environment preferred. Additional Information Intuitive ist ein Arbeitgeber, der gleiche und gerechte Beschäftigungsmöglichkeiten bietet. Wir bieten allen qualifizierten Bewerbern und Mitarbeitern gleiche Beschäftigungsmöglichkeiten, unabhängig von ethnischer Herkunft, Geschlecht, Schwangerschaft, sexueller Orientierung, Geschlechtsidentität, nationaler Herkunft, Hautfarbe, Alter, Religion, geschütztem Veteranenstatus, Behindertenstatus, genetischen Informationen oder einem anderen Status, der nach den geltenden Gesetzen auf Bundes-, Landes- oder lokaler Ebene geschützt ist, und verbieten jegliche Form von Diskriminierung und Belästigung. Gemäß den „Fair Chance“-Gesetzen berücksichtigen wir qualifizierte Bewerber, die verhaftet wurden oder Vorstrafen haben, für offene Stellen. Standort Intuitive, Pforzheim

Über unsWir sind eine mittelständische Unternehmensgruppe mit 20 Vertriebsgesellschaften in Europa, Nordamerika, Asien und Australien und beschäftigen insgesamt über 1.300 Mitarbeiter. Wir zählen weltweit zu den führenden Herstellern unserer Branche und exportieren unsere Produkte in über 120 Länder. Die Schwerpunkte unserer Fertigung sind Stanz- und Umformtechnik, Schweißen und Montage sowie Kunststoffverarbeitung. Unsere Kunden sind überwiegend Industriefirmen, die unsere Produkte in ihre Erzeugnisse einbauen sowie der technische Fachhandel.Eine seriöse, dynamische Geschäftspolitik, die Qualität unserer Produkte und ein gutes Betriebsklima sind die Grundlagen unseres anhaltenden Erfolges. Im Zuge einer Nachfolgeregelung suchen wir Sie als Export Area Manager / Area Sales Manager Export / Sales Specialist (m/w/d) - Asia-Pacific Standort: RosenfeldIhre AufgabenKompetenter Ansprechpartner für unsere internationale Kundschaft im Raum Asia-PacificTechnische Beratung und Abwicklung der Korrespondenz mit unseren Niederlassungen und internationalen VertriebspartnernAngebotserstellung und -verfolgungBetreuung von Besuchern und Reisetätigkeit in die betreuten Länder nach gründlicher EinarbeitungDurchführung von technischen ProdukttrainingsMitwirkung bei der Erarbeitung von Marktstrategien und dem weiteren Auf- und Ausbau unserer internationalen VertriebsorganisationIhr ProfilVertriebserfahrung im technischen Vertrieb von beratungsintensiven ProduktenAbgeschlossene kaufmännische Ausbildung, wie z. B. zum Kaufmann für Groß- und Außenhandelsmanagement (m/w/d), idealerweise in einem vertriebsnahen Umfeld sowie fundierte Berufserfahrung im internationalen Geschäft. Alternativ ein betriebswirtschaftliches oder technisches Studium, wie z. B. BWL-Handel, BWL-International Business oder Wirtschaftsingenieurwesen sowie Berufserfahrung im entsprechenden SegmentGutes technisches VerständnisKontaktfähigkeit und VerhandlungsgeschickKommunikationssicheres Englisch in Wort und SchriftKenntnisse asiatischer Sprachen sind von VorteilDienstsitz ist RosenfeldGültiger Führerschein Klasse BUnser AngebotKommen Sie an: Individuelle Einarbeitung in das entsprechende AufgabengebietGestalten Sie Ihre Zukunft: Mit spannenden Schulungs- und Weiterbildungsmöglichkeiten, die Sie beruflich und persönlich wachsen lassenProfitieren Sie von: Vielfältigen Mitarbeiterangeboten, wie Dienstrad-Leasing, Corporate Benefits, kostenfreie Wasserspender und einem abwechslungsreichen Speisenangebot im Blickle-BetriebsrestaurantBleiben Sie flexibel: Mit dem Blickle-Gleitzeitmodell, flexiblen Arbeitszeiten und unserer Homeoffice-RegelungWir sichern Sie ab: Langfristiger und sicherer Arbeitsplatz in einer expandierenden, zukunftsorientierten und gesunden mittelständischen UnternehmensgruppeWir bieten Ihnen: Eine angemessene Vergütung, Urlaubs- und Weihnachtsgeld, 30 Urlaubstage, eine faire Überstundenregelung und die Blickle ErfolgsprämieHaben wir Ihr Interesse geweckt?Dann freuen wir uns auf Ihre vollständige Bewerbung (Anschreiben, Lebenslauf, Zeugnisse), die Sie uns bitte in unserem Karriereportal zusenden. Für nähere Informationen steht Ihnen Herr Raumann (Telefon: 07428 932-191) gerne zur Verfügung.Blickle Räder + Rollen GmbH u. Co. KG Heinrich-Blickle-Str. 1 72348 Rosenfeld Germany Tel.: 07428 932-0 Fax: 07428 932-79191E-Mail anzeigenwww.blickle.com Standort Blickle Räder + Rollen GmbH u. Co. KG, Rosenfeld

Über unsWir sind eine mittelständische Unternehmensgruppe mit 20 Vertriebsgesellschaften in Europa, Nordamerika, Asien und Australien und beschäftigen insgesamt über 1.300 Mitarbeiter. Wir zählen weltweit zu den führenden Herstellern unserer Branche und exportieren unsere Produkte in über 120 Länder. Die Schwerpunkte unserer Fertigung sind Stanz- und Umformtechnik, Schweißen und Montage sowie Kunststoffverarbeitung. Unsere Kunden sind überwiegend Industriefirmen, die unsere Produkte in ihre Erzeugnisse einbauen sowie der technische Fachhandel.Eine seriöse, dynamische Geschäftspolitik, die Qualität unserer Produkte und ein gutes Betriebsklima sind die Grundlagen unseres anhaltenden Erfolges. Im Zuge einer Nachfolgeregelung suchen wir Sie als Export Area Manager / Area Sales Manager Export / Sales Specialist (m/w/d) - Asia-Pacific Standort: RosenfeldIhre AufgabenKompetenter Ansprechpartner für unsere internationale Kundschaft im Raum Asia-PacificTechnische Beratung und Abwicklung der Korrespondenz mit unseren Niederlassungen und internationalen VertriebspartnernAngebotserstellung und -verfolgungBetreuung von Besuchern und Reisetätigkeit in die betreuten Länder nach gründlicher EinarbeitungDurchführung von technischen ProdukttrainingsMitwirkung bei der Erarbeitung von Marktstrategien und dem weiteren Auf- und Ausbau unserer internationalen VertriebsorganisationIhr ProfilVertriebserfahrung im technischen Vertrieb von beratungsintensiven ProduktenAbgeschlossene kaufmännische Ausbildung, wie z. B. zum Kaufmann für Groß- und Außenhandelsmanagement (m/w/d), idealerweise in einem vertriebsnahen Umfeld sowie fundierte Berufserfahrung im internationalen Geschäft. Alternativ ein betriebswirtschaftliches oder technisches Studium, wie z. B. BWL-Handel, BWL-International Business oder Wirtschaftsingenieurwesen sowie Berufserfahrung im entsprechenden SegmentGutes technisches VerständnisKontaktfähigkeit und VerhandlungsgeschickKommunikationssicheres Englisch in Wort und SchriftKenntnisse asiatischer Sprachen sind von VorteilDienstsitz ist RosenfeldGültiger Führerschein Klasse BUnser AngebotKommen Sie an: Individuelle Einarbeitung in das entsprechende AufgabengebietGestalten Sie Ihre Zukunft: Mit spannenden Schulungs- und Weiterbildungsmöglichkeiten, die Sie beruflich und persönlich wachsen lassenProfitieren Sie von: Vielfältigen Mitarbeiterangeboten, wie Dienstrad-Leasing, Corporate Benefits, kostenfreie Wasserspender und einem abwechslungsreichen Speisenangebot im Blickle-BetriebsrestaurantBleiben Sie flexibel: Mit dem Blickle-Gleitzeitmodell, flexiblen Arbeitszeiten und unserer Homeoffice-RegelungWir sichern Sie ab: Langfristiger und sicherer Arbeitsplatz in einer expandierenden, zukunftsorientierten und gesunden mittelständischen UnternehmensgruppeWir bieten Ihnen: Eine angemessene Vergütung, Urlaubs- und Weihnachtsgeld, 30 Urlaubstage, eine faire Überstundenregelung und die Blickle ErfolgsprämieHaben wir Ihr Interesse geweckt?Dann freuen wir uns auf Ihre vollständige Bewerbung (Anschreiben, Lebenslauf, Zeugnisse), die Sie uns bitte in unserem Karriereportal zusenden. Für nähere Informationen steht Ihnen Herr Raumann (Telefon: 07428 932-191) gerne zur Verfügung.Blickle Räder + Rollen GmbH u. Co. KG Heinrich-Blickle-Str. 1 72348 Rosenfeld Germany Tel.: 07428 932-0 Fax: 07428 932-79191E-Mail anzeigenwww.blickle.com Standort Blickle Räder + Rollen GmbH u. Co. KG, Rosenfeld

About the jobUNOQUIP was founded on a simple idea: Expert Solutions to improve patient care. With experienced international partners, we are marketing and selling medical devices in the field of fluid management, respiratory care, airway management and nursing care.Are you ready to take on this mission? Reporting to the Commercial Head of DACH, you’ll take care of UNOQUIP's Clinical Sales and Business Development in Germany. The purpose of this position is to deliver real clinical value to health care professionals and business partners – go beyond product to improve patient outcomes.1. Who are we?Founded in October 2022, UNOQUIP is a fast-growing global marketer of high-quality single-use medical devices. We are dedicated to equipping healthcare professionals with solutions to provide optimal patient care in acute care settings.We are an international, experienced, and highly committed team with a passion for what we do. UNOQUIP strives to be recognized as experts in solutions for single-use medical devices. We work closely with our customers to deliver superior solutions, with exceptional service and with the clear purpose of improving patient outcomes.UNOQUIP is headquartered in Schaffhausen, Switzerland and has offices and direct presence in Spain, Denmark, Sweden, Norway, Finland, U.K. and Australia. UNOQUIP also collaborates closely with global distribution partners, all of whom have extensive medical device expertise and share our commitment to providing solutions that meet the needs of the healthcare sector. Distribution to our customers is organized from four distribution centers in Belgium, the UK, and Australia.What We Value:· Trust: We build relationships based on trust, internally and with our valued business partners.· Passion: We seek individuals who are passionate about making a difference in the healthcare industry.· Positive Mindset: A positive outlook is the key to finding the right solutions and overcoming challenges.2. What will you work on? You will be responsible for a wide range of responsibilities and tasks related to the direct clinical sales of UNOQUIP products in Germany, as well as liaising with our distribution partners in Austria and Switzerland. A key element of the role will be to provide clinical support to our business and Group Purchasing Organisation (GPO, Einkaufsgemeinschaften) strategy.You will work in an operational role and be responsible for building strong and sustainable relationships with healthcare professionals and decision makers, demonstrating an outstanding level of accountability with focus on customer needs and UNOQUIP's business objectives. This is an exciting opportunity to join a young organisation and make a significant and defining impact on our regional presence in the DACH region. 3. Your areas of knowledge and expertise (that matter most for this role):You will be responsible for the following areas:Maximising the clinical awareness for our products and their benefits, resulting in increased usage of our products in the region.Developing business concepts, total cost of care / budget impact models and perform other activities in line with our strategies, creating value for the customers and increasing UNOQUIPs footprint and sales.Adding the clinical angle to drive product- price and mix favourable for customers and UNOQUIP.Providing clinical training support and mentor your colleagues with continued education.Building and executing regional competitive growth strategies on focus products.Partnering with local teams and regional organisations (such as nursing associations) to conduct clinical events.Driving clinical projects from start to completion while utilizing project management skills to reach strategic objectives.Creating and developing innovative ways to reach and educate customers.Maintaining an understanding of current clinical regulations and common industry practices.Identifying and driving new business opportunities and ensure commercial clinical execution versus strategy.In this multifaceted, important position you will report directly to the commercial head of DACH while also have your own territory.4. You have / you are:Bachelor’s degree in Life Science or Business-related subjects or other relevant education.A strong clinical understanding, preferably a clinical nursing background in acute care.Strong, empathic presentation skills including presentations in front of clinical stakeholders.A talent to interact with healthcare professionals and operating in complex clinical environments like intensive care units.Proven ability to work within a team with a can-do attitude, being open for new experiences and changes.Good selling skills, while not necessarily being a sales expert.A talent for identifying trends and future requirements and being able to share and distribute the knowledge in a wider organisation.Experience of working in the Medical Device Industry will be an advantage.Through effective decision-making, planning, and implementation, deliver superior business results within tight deadlines.Analytical & IT skills, including ability to efficiently work with excel calculations and databases.Confident personality with an engaging positive mindset and attention to detail.Work with minimal supervision, good initiative, and follow-up, focus on details, while understanding how work fits into the larger picture.100% proficient in your local language (German), written and spoken, and in English.Other requirements:Ability to travel 50% of the working time.References from at least 2 senior managers and from 2 reputable customers.Desired:Experience in working in international organisations and/or project groups.Preferred experience in using MS Dynamics 365.5. What can we offer you?Engage in building an international medical device start-up with a strong patient focus and international colleagues.Be part of an energetic, collaborative, and positive culture.Basic and ongoing training in our product range and market trends, to enable competent exchanges with suppliers and customers.Become involved in a very meaningful project in the healthcare industry.Company car.Up to 28 days of vacation.Ability to work 100% remotely.6. Interested?Complete the LinkedIn application.We aim to give you an initial response within 2 weeks. Next steps are communicated in the phone call with recruiters.As a candidate, you consent to UNOQUIP storing your CV and application for the purpose of recruiting for the specific positions advertised here. We will keep the data for a maximum of 6 months, during which time you can also ask us to delete your data by writing us through Linkedin with subject “GDPR - Your full Name”. Standort UNOQUIP, Stuttgart

Clinical Study Nurse at ClinChoice (View all jobs) Tübingen, Germany Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds.... ClinChoice is searching for a Clinical Study Nurse to join one of our clients, where you will work on-site at a hospital in Tübingen, initially 0.5 FTE for a 12 month contract. ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts. Main Job Tasks and Responsibilities: Measure vital signs (i.e. blood pressure, pulse rate, BMI, etc.), perform ECG’s, draw blood and perform infusions including putting infusion tubes and clinical monitoring during/after the infusion. Ship blood and laboratory samples to the central labs. Check questionnaires, perform database screening and discuss study information with subjects to aid with informed consent. Support the Principal Investigator with subject eligibility. Maintain Investigator Site File. Assist project teams with study-specific documentation as appropriate. Complete Case Report Forms (CRFs/eCRFs) and Data Clarification Forms (DCFs). Track, quality check and maintain drug accountability records. Ensure completion of site status reports. Ensure source documents (e.g. laboratory reports) are reviewed and signed by The Investigator. Maintain study files and the databases for assigned projects. Co-coordinate ordering/dispatch and track trial materials. Assist with trial progress tracking and update distribution tasks by updating the Clinical Trial Management systems. Support with tracking and safety reporting of study progress. Provide activity reports, expenses and timesheets as required. Report adverse events (AEs) and serious adverse events (SAEs) to all relevant personnel parties. Enter data into the eCRF. Work with the Clinical Research Associate (CRA) to resolve queries. Adhere to the site and study-specific protocol training whilst undertaking visit duties. Maintain standards of professional competence and current clinical practices under ICG-GCP, EU Clinical Trials Directive EU2001/20EC and German Regulatory Requirements. Complete study visits at the site, in line with the study protocol requirements. Ensure all relevant information regarding subjects is recorded, reported and where necessary, acted upon the communicate any changes to the Investigator study team as appropriate. Work at site and Patient Services team to ensure that all aspects of service for assigned groups of subjects are met, through the adherence to study schedules, protocols and local clinical practice regulations and requirements. Flexible approach to working hours to accommodate the dynamic nature of research visits. Education and Experience: Registered Nurse or Medical Assistant with at least 2 years of post-registration experience. Previous experience as a Research Nurse or Medical Assistant including a recent (within the last 1 year) ICH-GCP update. Experience in neurology is desirable. Skills Requirements: Infusion experience essential. Good phlebotomy skills. ECG recording. Managing infusion reactions. Demonstrated organisational skills. Proven flexibility and the ability to work under pressure. Good communication skills. Proficiency in German mandatory, English desirable. Proactive contribution towards the team by being a flexible team player. Ability to work effectively both in a team & independently in a fast-paced environment. Excellent understanding of the clinical processes. Good knowledge of clinical trials, including EU Clinical Trials Directives, Good Clinical Practice for Clinical Trials, and German regulations is desirable, training can be provided. Excellent computer skills required, MS Office proficiency at a minimum. The Application ProcessOnce you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for 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. Who will you be working for? About ClinChoiceClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company EthosOur mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice 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. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key words: Study Nurse, Research Nurse, Trial Nurse, Registered Nurse, Clinical Trials, Clinical Research, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated #LI-DNP

Clinical Study Nurse at ClinChoice (View all jobs) Tübingen, Germany Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds.... ClinChoice is searching for a Clinical Study Nurse to join one of our clients, where you will work on-site at a hospital in Tübingen, initially 0.5 FTE for a 12 month contract. ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts. Main Job Tasks and Responsibilities: Measure vital signs (i.e. blood pressure, pulse rate, BMI, etc.), perform ECG’s, draw blood and perform infusions including putting infusion tubes and clinical monitoring during/after the infusion. Ship blood and laboratory samples to the central labs. Check questionnaires, perform database screening and discuss study information with subjects to aid with informed consent. Support the Principal Investigator with subject eligibility. Maintain Investigator Site File. Assist project teams with study-specific documentation as appropriate. Complete Case Report Forms (CRFs/eCRFs) and Data Clarification Forms (DCFs). Track, quality check and maintain drug accountability records. Ensure completion of site status reports. Ensure source documents (e.g. laboratory reports) are reviewed and signed by The Investigator. Maintain study files and the databases for assigned projects. Co-coordinate ordering/dispatch and track trial materials. Assist with trial progress tracking and update distribution tasks by updating the Clinical Trial Management systems. Support with tracking and safety reporting of study progress. Provide activity reports, expenses and timesheets as required. Report adverse events (AEs) and serious adverse events (SAEs) to all relevant personnel parties. Enter data into the eCRF. Work with the Clinical Research Associate (CRA) to resolve queries. Adhere to the site and study-specific protocol training whilst undertaking visit duties. Maintain standards of professional competence and current clinical practices under ICG-GCP, EU Clinical Trials Directive EU2001/20EC and German Regulatory Requirements. Complete study visits at the site, in line with the study protocol requirements. Ensure all relevant information regarding subjects is recorded, reported and where necessary, acted upon the communicate any changes to the Investigator study team as appropriate. Work at site and Patient Services team to ensure that all aspects of service for assigned groups of subjects are met, through the adherence to study schedules, protocols and local clinical practice regulations and requirements. Flexible approach to working hours to accommodate the dynamic nature of research visits. Education and Experience: Registered Nurse or Medical Assistant with at least 2 years of post-registration experience. Previous experience as a Research Nurse or Medical Assistant including a recent (within the last 1 year) ICH-GCP update. Experience in neurology is desirable. Skills Requirements: Infusion experience essential. Good phlebotomy skills. ECG recording. Managing infusion reactions. Demonstrated organisational skills. Proven flexibility and the ability to work under pressure. Good communication skills. Proficiency in German mandatory, English desirable. Proactive contribution towards the team by being a flexible team player. Ability to work effectively both in a team & independently in a fast-paced environment. Excellent understanding of the clinical processes. Good knowledge of clinical trials, including EU Clinical Trials Directives, Good Clinical Practice for Clinical Trials, and German regulations is desirable, training can be provided. Excellent computer skills required, MS Office proficiency at a minimum. The Application ProcessOnce you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for 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. Who will you be working for? About ClinChoiceClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company EthosOur mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice 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. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key words: Study Nurse, Research Nurse, Trial Nurse, Registered Nurse, Clinical Trials, Clinical Research, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated #LI-DNP

Ihr Aufgabenbereich -Sie planen und führen Lieferantenbesuche, Potenzialanalysen und Lieferantenaudits durch-Sie sind für die Betreuung und die strategische Entwicklung von nationalen und internationalen Lieferanten im Rahmen der zugeordneten Materialgruppe zuständig-Sie betreuen die Qualität sowie die Weiterentwicklung der neuen und vorhandenen Lieferanten-Die Vorbereitung, Verhandlung und Abschluss von Qualitätsverträgen sowie die Zulassung und Qualifizierung der Lieferanten liegt in Ihrer Hand-Sie gestalten bei der Umsetzung der Qualitätsanforderungen unter Anwendung gängiger Q-Methoden und Normen (z.B. ISO9001, EN9100, IATF 16949)-Teamleitung zur strukturierten Problemlösungen (QRQC)-Sie sind die Schnittstelle zu Lieferanten sowie intern zu den Bereichen Entwicklung, Produktion und Einkauf Ihr Profil -Sie haben ein erfolgreich abgeschlossenes Studium im Bereich Elektronik, Elektrotechnik oder vergleichbares-Sie besitzen Berufserfahrung im Qualitätsmanagement von Elektronikprodukten-Sie besitzen praktische Erfahrung in der Fertigung von Elektronikprodukten in der Zusammenarbeit mit EMS-Dienstleistern-Sie haben die Zusatzqualifikation sowie die Erfahrung als Auditor (z. B. VDA 6.3, IAFT 16949, ISO 19011)-Sie gehen sicher im Umgang mit Lieferanten und Geschäftspartnern um-Sie besitzen Kommunikationsstärke-Ihre sehr guten Deutsch- und Englischkenntnisse runden Ihr Profil abAuf Ihre Bewerbung freuen wir uns.Tel. +49 (0)751 56 84 97 30E-Mail: [email protected]

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Roles & Responsibilities of the position: The Trial Manager (m/f/d) is responsible for the management of clinical sites including the site identification and qualification, the timely delivery of clinical trial enrollment in accordance with scientific objectives, timely delivery of database locks, issues management at clinical trial sites, and ensuring inspection readiness at all times for assigned therapeutic areas within a region or country. You will also be responsible for the oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends. Key Responsibilities: You will be responsible for all activities required at clinical trial sites and by investigators and site staff participating in the client’s trials; including the site identification and qualification, enrollment planning and execution, to database lock and close out You will also perform management and issue mitigation, identification and resolution The development of strategic institutional/site relationships will be a main focus You will develop and implement site risk plans, ensure site and country level inspection readiness at all times, leverage metrics to inform site/country/regional level for their decision making and provide vendor oversight for site monitoring activities at site/country level It will be a goal to establish and develop strong professional relationships with clinical investigators All in all you will be the communication “bridge” between sites, third party vendors and the client Job Requirements: You have a Bachelor’s degree or equivalent in a scientific or health-related field You also bring experience in clinical research as well as good GCP knowledge Demonstrated leadership behavior, strong communication skills as well as the willingness to travel are also required About 4 + years of experience in clinical trial monitoring or similar experience in the industry A very good professional knowledge of German and English