JOTEC GmbH
72379 Hechingen - Deutschland
Referent/in - klinische Studien (CRA)
Arbeit
Vollzeit
ab 04.12.2025
Beschreibung
It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together.
We are hiring a
**Senior Clinical Research Project Manager (m/f/d) – EMEA**
## Your Strength
- Bachelor’s degree in biological sciences, engineering, or related field
- Minimum of 5 years’ experience planning and executing clinical research studies, or 3 years with an advanced degree
- Proven ability to manage multicenter clinical studies in Europe and APAC (ie pre or post market clinical investigations) Strong project management, communication, and critical thinking skills
- Proficient in medical terminology and Microsoft Office tools (Excel, PowerPoint, Word, Project)
- Experience with clinical documentation, protocol design, and investigator communication
- Fluent in English; additional language skills are a plus
- Willingness to travel up to 30% (domestically and internationally)
## Your Contribution
- Independently lead all phases of clinical study management (protocol development to final reporting)
- Serve as main point of contact for monitors, sites, CROs, and other clinical stakeholders
- Draft, review, and manage study documents: protocols, CRFs, informed consents, site manuals, etc.
- Coordinate study timelines, budgets, resources, and vendors
- Ensure audit readiness and compliance clinical regulatory bodies (ie NCAs and Ecs)
- Collaborate with Quality, Regulatory, Medical Affairs, and Finance teams
- Manage site qualification, initiation, training, and issue resolution
- Lead internal and external study team meetings and communication
- Support centralized data reviews and CRF reconciliation
- Develop and maintain training materials and deliver HCP presentations
- Proactively assess and mitigate study-related risks
- Contribute to clinical reports and collaborate with statisticians
## Our Strength
- A mission-driven Clinical Research team with international collaboration
- High-impact work in cutting-edge cardiovascular studies
- Structured onboarding and continuous professional development
- Flexible work environment and opportunities to grow
- Competitive compensation and benefits including pension plan and EGYM Wellpass
## Contact
Apply now and join the Artivion Team. We are looking forward to receiving your application documents in English directly via our online system.
Brian Russo,T: +41 435 08 39 01
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
[www.artivion.com](http://www.artivion.com/)
We are hiring a
**Senior Clinical Research Project Manager (m/f/d) – EMEA**
## Your Strength
- Bachelor’s degree in biological sciences, engineering, or related field
- Minimum of 5 years’ experience planning and executing clinical research studies, or 3 years with an advanced degree
- Proven ability to manage multicenter clinical studies in Europe and APAC (ie pre or post market clinical investigations) Strong project management, communication, and critical thinking skills
- Proficient in medical terminology and Microsoft Office tools (Excel, PowerPoint, Word, Project)
- Experience with clinical documentation, protocol design, and investigator communication
- Fluent in English; additional language skills are a plus
- Willingness to travel up to 30% (domestically and internationally)
## Your Contribution
- Independently lead all phases of clinical study management (protocol development to final reporting)
- Serve as main point of contact for monitors, sites, CROs, and other clinical stakeholders
- Draft, review, and manage study documents: protocols, CRFs, informed consents, site manuals, etc.
- Coordinate study timelines, budgets, resources, and vendors
- Ensure audit readiness and compliance clinical regulatory bodies (ie NCAs and Ecs)
- Collaborate with Quality, Regulatory, Medical Affairs, and Finance teams
- Manage site qualification, initiation, training, and issue resolution
- Lead internal and external study team meetings and communication
- Support centralized data reviews and CRF reconciliation
- Develop and maintain training materials and deliver HCP presentations
- Proactively assess and mitigate study-related risks
- Contribute to clinical reports and collaborate with statisticians
## Our Strength
- A mission-driven Clinical Research team with international collaboration
- High-impact work in cutting-edge cardiovascular studies
- Structured onboarding and continuous professional development
- Flexible work environment and opportunities to grow
- Competitive compensation and benefits including pension plan and EGYM Wellpass
## Contact
Apply now and join the Artivion Team. We are looking forward to receiving your application documents in English directly via our online system.
Brian Russo,T: +41 435 08 39 01
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
[www.artivion.com](http://www.artivion.com/)
Quelle: Bundesagentur für Arbeit - Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
Ref-Nr.: a1b9238cf50c634ff71b3510454ba20a
Letztes Update:
14.12.2025
Passende Jobs für dich
Uniklinik RWTH Aachen
52062 Aachen
Arbeit
ab 01.12.2025
Roche Diagnostics GmbH
79639 Grenzach-Wyhlen
Arbeit
ab 01.02.2026
MEDICE Arzneimittel Pütter GmbH & Co. KG
58638 Iserlohn
Arbeit
ab 10.12.2025
Thermo Fisher Scient. Messt. GmbH
80333 München
Arbeit
ab 12.12.2025
Alcedis GmbH
35394 Gießen, Lahn
Arbeit
ab 01.12.2025
