We are hiring a
Your Strength
- 2-4 years of relevant professional experience in clinical or medical writing
- Strong organizational skills and attention to detail
- Ability to interpret and explain scientific data from various sources including studies, literature, and technical documentation
- Excellent command of written and spoken English
- Proficiency in medical literature research, data analysis, and content development
- Experience collaborating with cross-functional teams such as Clinical, R&D, Quality, and Regulatory Affairs
- Experience with EU MDR (Medical Device Regulation), including familiarity with Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), Post-Market Clinical Follow-up (PMCF) plans, and other clinical evidence documents is an advantage
Your Contribution
- Draft, edit, proofread, and manage clinical documents such as CERs, CEPs, PMCF Plans, scientific articles and others
- Collaborate under supervision on moderately complex projects or support senior medical writers
- Coordinate document timelines and ensure timely delivery
- Conduct literature searches and appraisals in alignment with clinical and regulatory needs
- Assist in aligning documentation with risk/benefit assessments, current scientific literature, and regulatory standards
- Support meetings and communication related to clinical content and investigator materials
- Work closely with internal stakeholders (Clinical, R&D, RA/QA, Marketing) and external partners (surgeons, consultants, CROs)
Our Strength
- A mission-driven, international work environment focused on innovation and quality
- Exciting projects with a global impact in the medical device industry
- Career development opportunities, including training programs and support for continuing education
- Flexible working models, including hybrid options
- Attractive benefits including pension schemes, EGYM Wellpass, and more
Contact
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com
