You create and manage clinical documents, collaborate on projects, and conduct literature searches, ensuring compliance with regulatory standards and facilitating effective communication across teams.
Anforderungen
- •2–4 years of relevant experience
- •Strong organizational skills
- •Ability to interpret scientific data
- •Excellent command of English
- •Proficiency in medical literature research
- •Experience collaborating with cross-functional teams
- •Familiarity with EU MDR is an advantage
Deine Aufgaben
- •Draft, edit, and proofread clinical documents.
- •Manage clinical documents such as CERs and PMCF Plans.
- •Collaborate on projects with guidance from senior writers.
- •Coordinate document timelines for timely delivery.
- •Conduct literature searches for clinical and regulatory needs.
- •Align documentation with risk/benefit assessments.
- •Support meetings on clinical content and investigator materials.
- •Work with internal and external stakeholders effectively.
Deine Vorteile
Mission-driven international environment
Exciting global impact projects
Career development opportunities
Flexible working models
Attractive benefits package
Original Beschreibung
# Medical Writer (m/f/d)
* Hechingen
* Medizin, Pharmazie, Labor
* Publiziert: 21.05.2025
## Introduction
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
**Medical Writer (m/f/d)**
Location: Hechingen, Germany or Remote (Europe)
## 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