Senior PSUR Writer
CooperSurgical · United States · US
Medical Writing
Remote
Not yet analysed
Demand78
Career growth75
Healthcare fit72
Remote potential95
5-year outlook
Senior regulatory and medical writing roles in medical devices are likely to remain in demand due to evolving post-market surveillance regulations; compensation should be competitive for experienced writers, though exact figures vary by location and experience.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-04
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for clinicians with regulatory, pharmacovigilance, or medical writing experience who want a remote non-clinical career; not suitable for those without prior PSUR/PMSR or regulatory documentation exposure.
Who should apply
Pharmacists, nurses, physicians, and allied health professionals with clinical safety, pharmacovigilance, regulatory affairs, or medical writing backgrounds, especially those experienced in adverse event reporting or clinical documentation.
CV angle
Reframe clinical experience as evidence of safety reporting, adverse event documentation, literature evaluation, regulatory compliance, and cross-functional collaboration; highlight any experience with PSURs, PMS, medical writing, or regulatory submissions without fabricating.
Skills to highlight
- Post-market surveillance
- PSUR/PMSR/PMSP writing
- Regulatory compliance
- Medical writing
- Risk-benefit analysis
- Safety signal detection
- Project management
- Cross-functional collaboration
Role summary
A senior remote medical writing and regulatory role responsible for authoring and coordinating post-market surveillance plans and periodic safety reports for medical devices, ensuring global regulatory compliance and supporting junior writers.
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