Senior Clinical Project Manager (m/f/d)

  • Jotec GmbH Jobportal
  • Kaufmännische Berufe (Sonstige)
  • Publiziert: 21.05.2025
Senior Clinical Project Manager (m/f/d), 1. Bild
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) 
 
Location: Hechingen, Germany or Remote (Europe)

Your Strength

  • Bachelor’s degree in biological sciences, engineering 
  • Experience in Medical Devices (Plus)
  • At least 5 years of experience in planning and executing clinical research studies or 3+ years with an advanced degree
  • Proven track record of managing multicenter investigational (e.g. IDE) studies preferably medical device studies
  • Strong project management and analytical skills with the ability to think critically and communicate effectively
  • In-depth knowledge of medical terminology and clinical documentation
  • Proficient in MS Office (Excel, Word, PowerPoint), project management tools, and web-based applications
  • Ability to travel domestically and internationally up to 30% of the time
  • Fluency in English

Your Contribution

  • Lead the development and management of clinical research projects from study design to close-out
  • Create and oversee clinical study documentation (e.g. protocols, CRFs, informed consents, investigator manuals)
  • Act as primary contact for internal and external stakeholders including CROs, sites, monitors, and data managers
  • Coordinate and lead study team meetings, ensuring timeline adherence and risk mitigation
  • Submit studies to ethics committees/IRBs and manage responses to regulatory bodies
  • Ensure negotiation and finalization of clinical Study Agreements as per study budget and applicable regulation
  • Define and ensure fulfillment of adequate safety reporting as per local requirements
  • Collaborate with cross-functional teams including Quality, RA/QA, and Finance
  • Manage vendor selection and contract processes, including budget tracking and oversight
  • Support and ensure audit readiness, compliance, and proper documentation across all project stages
  • Contribute to clinical study reports and data verification processes in collaboration with statisticians
  • Contribute to internal and external communications (e.g. oral presentations, written publications)

Our Strength

  • A dynamic, international work environment with opportunities for innovation and leadership
  • Diverse and challenging projects with significant global impact
  • Opportunities for career growth and specialized training programs
  • Flexible working conditions, including hybrid options

Contact

Apply now and join the Artivion team. We are looking forward to receiving your application documents 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