Senior Medical Writer - Clinical Evaluation Reporting (CER)
Abbott · Maple Grove, MN +4 more
The apply link worked recently (not employer-confirmed).
Role summary
Abbott seeks a Senior Medical Writer to develop clinical evaluation documentation for neuromodulation, cardiovascular, and vascular products across multiple U.S. locations. The role involves authoring regulatory reports, synthesizing clinical evidence, and collaborating with cross-functional teams to support product development and regulatory submissions. Candidates should have experience in clinical study design, medical writing, or quality engineering with strong communication skills.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-08-19). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Bachelor's degree in science, medical technology, or equivalent technical field
- Minimum 3 years relevant experience in R&D, technical product development, or quality in healthcare
- Strong written and verbal communication, analytical, and project management skills
- Experience writing, editing, and managing engineering and technical documentation
- Experience with complaint handling, diagnostic instrumentation, or medical technology
- Advanced degree in science, biomedical engineering, medicine, or nursing preferred
- 3+ years medical writing in medical device/pharmaceutical industry or 7+ years general technical writing with CER experience preferred
What you'll be doing
- Author and contribute to Clinical Evaluation Plans, Reports, PMS, PMCF, and regulatory submission documents
- Evaluate and summarize clinical evidence from investigations, literature, surveillance, and post-market data for product applications
- Collaborate with cross-functional teams including regulatory affairs, quality, clinical affairs, and R&D on CER projects
- Review Instructions for Use, patient guides, risk management files, and clinical protocols for alignment and consistency
- Ensure quality, compliance, and data integrity across all deliverables and regulatory communications
Privacy & handoff
This role links to Abbott's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.