Medical Trials Stellenangebote


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302 Jobs für Medical Trials


Stellenangebote Medical Trials Jobs


Job vor 13 Tagen bei StepStone gefunden KWS Group

Crop Protection Expert ( (m/w/d) / w) Product Mgmt Agroservice Poland

• Poznan Homeoffice möglich [. .. ] and implement strategies to manage weed and fungal pathogen resistance in sugar beet production by promoting sustainable crop rotation and optimized herbicide and fungicide programs. Plan, establish, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and manage field trials across Poland, analyze results, and provide technical recommendations. Monitor herbicide and fungicide resistance, collect field samples, and collaborate with KWS headquarters and international experts to support resistance monitoring and solution development. Transfer global technical knowledge and best practices to the Polish market and contribute to continuous innovation. Prepare and deliver [. .. ] international experts and participation in global projects Continuous professional development through training, knowledge sharing, and access to the international KWS network. Competitive salary and an attractive benefits package, including private medical care, life insurance, pension plan, additional vacation days, company laptop, and mobile phone A collaborative, respectful, and supportive working environment where your ideas and expertise matter A hybrid working model that offers flexibility while supporting close collaboration with colleagues and customers At KWS, we believe innovation starts with people. If [. .. ]

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Job am 14.08.2026 bei StepStone gefunden GALDERMA Laboratorium GmbH Senior Medical Science Liaison Dermatology (m/w/d) Sachsen-Brandenburg Süd • Leipzig, Sachsen, Brandenburg Abgeschlossenes Studium Betriebliche Altersvorsorge 30+ Urlaubstage [. .. ] führende Unternehmen für Dermatologie weltweit zu werden. Mit uns haben Sie die ultimative Möglichkeit, neue und herausfordernde Arbeitserfahrungen zu sammeln und einen beispiellosen direkten Einfluss zu erzielen. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Aufgaben Als Senior Medical Science Liaison Dermatology (m/w/d) übernehmen Sie die medizinisch-wissenschaftliche Betreuung des biologischen Arzneimittels Nemolizumab. Sie fördern den wissenschaftlichen Austausch mit medizinischen Expertinnen und Experten, unterstützen medizinische Projekte und tragen zur Umsetzung der Medical-Affairs-Strategie bei. Sie sind zentrale Ansprechperson für medizinische Expertinnen und Experten sowie interne Fachbereiche [. .. ] Boards und Scientific Dinners, unterstützen wissenschaftliche Symposien und halten Präsentationen sowie Schulungen für Healthcare Professionals (HCPs) und interne Teams. Sie begleiten medizinische Projekte wie nicht-interventionelle Studien und Investigator Initiated Trials und fördern den wissenschaftlichen Austausch mit externen Partnern. Sie arbeiten eng mit Medical Affairs, Marketing, Regulatory und Vertrieb zusammen und stellen dabei die medizinische Unabhängigkeit sicher. Sie analysieren wissenschaftliche Erkenntnisse, Kongressinhalte und Marktinformationen, gewinnen relevante Field Insights und leiten daraus Handlungsempfehlungen ab. Sie beantworten qualifiziert medizinisch-wissenschaftliche Anfragen und beraten [. .. ]

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Job vor 8 Tagen bei Mindmatch.ai gefunden Randstad Belgium

Clinical Research Associate

• Berlin, BE Angebote von Zeitarbeitsunternehmen Freelance Clinical Research Associate (CRA) Germany Medical Devices Are you an experienced Clinical Research Associate looking for your next high-impact freelance project in the medical device sector? Do you thrive [...]
MEHR INFOS ZUM STELLENANGEBOT[...] in a hybrid role that combines the comfort of working from home with the energy of on-site hospital visits? Randstad Professional is seeking an autonomous [. .. ] a global healthcare leader and make a tangible impact on patient care. Job Content As a Freelance CRA, you will play a pivotal role in driving the success of clinical trials within the medical device sector. You will serve as the primary link between the sponsor and various investigator sites. This is a highly flexible freelance project with an average monthly resource requirement ranging from 50 to 100 of a full-time position. We welcome applicants with differing availabilities, as we [. .. ]

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Job vor 11 Tagen bei Mindmatch.ai gefunden Upsilon Global Clinical Research Associate • Leipzig, SN [. .. ] solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior Clinical Research Associates to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] support oncology clinical trials across Germany. This is an excellent opportunity for independent CRAs looking for a flexible contract assignment with a commitment of approximately 0.50.8 FTE. The Role As a Senior CRA, you will take responsibility for the monitoring and oversight of clinical trial sites, ensuring studies are conducted in accordance [. .. ] independent monitoring experience. Previous experience as a CRA or Senior CRA managing clinical trial sites independently. Oncology clinical trial experience is highly desirable. Experience within a CRO, pharmaceutical, biotechnology or medical device environment is preferred. Strong knowledge of ICH-GCP and EU clinical trial regulations, with familiarity with German regulatory requirements. Demonstrated experience conducting SIVs, IMVs/ RMVs and COVs. Experience supporting studies from start-up through to close-out. Strong experience with site management, regulatory documentation and TMf/e TMF processes. Proficiency [. .. ]

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Job vor 11 Tagen bei Mindmatch.ai gefunden Upsilon Global Clinical Research Associate • Cologne, NW [. .. ] solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior Clinical Research Associates to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] support oncology clinical trials across Germany. This is an excellent opportunity for independent CRAs looking for a flexible contract assignment with a commitment of approximately 0.50.8 FTE. The Role As a Senior CRA, you will take responsibility for the monitoring and oversight of clinical trial sites, ensuring studies are conducted in accordance [. .. ] independent monitoring experience. Previous experience as a CRA or Senior CRA managing clinical trial sites independently. Oncology clinical trial experience is highly desirable. Experience within a CRO, pharmaceutical, biotechnology or medical device environment is preferred. Strong knowledge of ICH-GCP and EU clinical trial regulations, with familiarity with German regulatory requirements. Demonstrated experience conducting SIVs, IMVs/ RMVs and COVs. Experience supporting studies from start-up through to close-out. Strong experience with site management, regulatory documentation and TMf/e TMF processes. Proficiency [. .. ]

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Job vor 11 Tagen bei Mindmatch.ai gefunden Upsilon Global Clinical Research Associate • Munich, BY [. .. ] solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior Clinical Research Associates to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] support oncology clinical trials across Germany. This is an excellent opportunity for independent CRAs looking for a flexible contract assignment with a commitment of approximately 0.50.8 FTE. The Role As a Senior CRA, you will take responsibility for the monitoring and oversight of clinical trial sites, ensuring studies are conducted in accordance [. .. ] independent monitoring experience. Previous experience as a CRA or Senior CRA managing clinical trial sites independently. Oncology clinical trial experience is highly desirable. Experience within a CRO, pharmaceutical, biotechnology or medical device environment is preferred. Strong knowledge of ICH-GCP and EU clinical trial regulations, with familiarity with German regulatory requirements. Demonstrated experience conducting SIVs, IMVs/ RMVs and COVs. Experience supporting studies from start-up through to close-out. Strong experience with site management, regulatory documentation and TMf/e TMF processes. Proficiency [. .. ]

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Job vor 11 Tagen bei Mindmatch.ai gefunden Upsilon Global Clinical Research Associate • Hamburg, HH [. .. ] solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior Clinical Research Associates to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] support oncology clinical trials across Germany. This is an excellent opportunity for independent CRAs looking for a flexible contract assignment with a commitment of approximately 0.50.8 FTE. The Role As a Senior CRA, you will take responsibility for the monitoring and oversight of clinical trial sites, ensuring studies are conducted in accordance [. .. ] independent monitoring experience. Previous experience as a CRA or Senior CRA managing clinical trial sites independently. Oncology clinical trial experience is highly desirable. Experience within a CRO, pharmaceutical, biotechnology or medical device environment is preferred. Strong knowledge of ICH-GCP and EU clinical trial regulations, with familiarity with German regulatory requirements. Demonstrated experience conducting SIVs, IMVs/ RMVs and COVs. Experience supporting studies from start-up through to close-out. Strong experience with site management, regulatory documentation and TMf/e TMF processes. Proficiency [. .. ]

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Job am 07.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Leipzig, SN Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden IQVIA

Senior Clinical Site Contracting Consultant, Med Tech

• Berlin, BE Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Leipzig, SN [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC)

Site Engagement Manager, Immunology (Germany)

• Frankfurt [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Berlin, BE [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Dortmund, NW [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Dortmund, NW Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Cologne, NW Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Munich, BY [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Hamburg, HH Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Düsseldorf, NW Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Cologne, NW [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Hamburg, HH [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 06.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Düsseldorf, NW [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 05.09.2026 bei Mindmatch.ai gefunden The Medical Affairs Company (TMAC) Site Engagement Manager, Immunology (Germany) • Essen, NW [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ]

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Job am 05.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Essen, NW Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 05.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Frankfurt Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Job am 05.09.2026 bei Mindmatch.ai gefunden IQVIA Senior Clinical Site Contracting Consultant, Med Tech • Munich, BY Beratungs-/ Consultingtätigkeiten [. .. ] Site Contracting Consultant, Med Tech to serve as a senior strategic point of contact for site contract template development, clinical site contract negotiations, escalation management, and contract [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution across European medical device clinical studies. This individual will bring deep expertise in site contracting, clinical trial agreements, and stakeholder management, partnering with sponsors, hospitals, health systems, and investigative sites to support study start-up and trial execution. The successful candidate will provide oversight on site agreement and budget development based on country [. .. ] Exceptional communication, negotiation, stakeholder management, and problem-solving skills. Ability to manage multiple studies and priorities within a fast-paced consulting environment. Preferred Experience Experience supporting European medical device clinical trials, clinical investigations, PMCF studies, registries, or real-world evidence programs. Bilingual in English, Dutch, French, Italian, or Spanish is preferred. Experience within a Med Tech CRO, sponsor organization, or strategic consulting environment. Knowledge of EU MDR requirements and device development lifecycle. Experience supporting multinational European studies across multiple therapeutic and [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Medical Trials pro Jahr?

Als Medical Trials verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Medical Trials Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 302 offene Stellenanzeigen für Medical Trials Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Medical Trials Jobs?

Aktuell suchen 35 Unternehmen nach Bewerbern für Medical Trials Jobs.


Welche Unternehmen suchen nach Bewerbern für Medical Trials Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Trials Stellenangebote:


  • IQVIA (25 Jobs)
  • Upsilon Global (12 Jobs)
  • Novartis (6 Jobs)
  • SCIRENT Clinical Research and Science (3 Jobs)
  • Phia LLC (2 Jobs)


In welchen Bundesländern werden die meisten Medical Trials Jobs angeboten?

Die meisten Stellenanzeigen für Medical Trials Jobs werden derzeit in Nordrhein-Westfalen (28 Jobs), Berlin (24 Jobs) und Niedersachsen (20 Jobs) angeboten.


Zu welchem Berufsfeld gehören Medical Trials Jobs?

Medical Trials Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.


Weitere Job-Ideen!
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