Senior Clinical Research Project Manager (m/f/d) – EMEA

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 #J-18808-Ljbffr