Clinical Project Manager (m/f/d)
- Jotec GmbH Jobportal
- Hechingen
- Publiziert: 15.04.2025
Clinical Project Manager (m/f/d)
Your Strength
- Bachelor’s degree in biological science, engineering, or a related scientific field
- Minimum 2 years of experience in planning and executing clinical research studies (or an advanced degree with at least 1 year of experience)
- Experience with multicenter investigational studies (e.g. IDE/pre-CE)
- Strong project management and critical thinking skills
- Proficient in medical terminology and clinical research regulations
- Experience with Ethic Committee submissions and vendor/site management
- Fluent in English (German is a plus)
- Proficient in Microsoft Office (Excel, PowerPoint, Word, Project) and web-based tools
- Willingness to travel up to 30% internationally and domestically
Your Contribution
- Manage clinical study activities and collaborate with investigators and research sites
- Support regulatory submissions and maintain EC approvals throughout the study
- Negotiate contracts and budgets with sites and vendors
- Provide training to clinical site staff and internal stakeholders
- Collaborate on the creation and dissemination of core clinical documentation
- Monitor data quality and ensure site compliance with protocols and contractual terms
- Contribute to cross-functional team efforts in clinical trial planning and execution
- Assist in the evaluation of clinical data and review CRA visit reports
Our Strength
- A dynamic, international work environment with opportunities for growth
- A collaborative and purpose-driven team committed to innovation in healthcare
- Flexible working conditions, including hybrid options
- Employee benefits such as pension plans, EGYM Wellpass, and career development support
Contact
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com