Senior Medical Writer/Principal Medical Writer
Precision for Medicine · Poland
Medical Writing
Remote
physician
Nurse
Pharmacist
Demand80
Career growth75
Healthcare fit85
Remote potential85
5-year outlook
Senior and Principal medical writers in CROs and sponsors typically have strong earning potential and can advance into lead or management roles; compensation varies by location, therapeutic area, and experience.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-03
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Profession fit
- physician, Nurse, Pharmacist
- 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 established medical writing experience in CRO or sponsor settings, especially in oncology or rare disease; not suitable for those without prior medical writing experience.
Who should apply
Physicians, pharmacists, nurses, or healthcare graduates with 5+ years of medical writing experience in a CRO or sponsor environment, ideally with oncology/rare disease and CSR/protocol experience.
CV angle
Frame clinical training and trial experience around regulatory document authorship, protocol and CSR development, data interpretation, QC, and cross-functional collaboration; highlight therapeutic areas, document types, and compliance with ICH/FDA/GCP/eCTD.
Skills to highlight
- Medical writing
- Clinical study protocols
- Clinical Study Reports (CSRs)
- Regulatory compliance (ICH, FDA, GCP)
- eCTD submissions
- QC review
- Document management
- Oncology/rare disease
Role summary
Lead the planning, writing, editing, and QC of clinical regulatory documents—including protocols, IBs, ICFs, DSURs, CSRs, and patient narratives—for a CRO/consulting firm, ensuring compliance with SOPs, regulatory guidelines, and eCTD requirements.
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