Sr ICF Medical Writing Project Manager
Thermo Fisher Scientific · Remote, Serbia · Global
Medical Writing
Remote
Not yet analysed
Demand68
Career growth62
Healthcare fit70
Remote potential65
5-year outlook
CRO medical writing and document project management roles typically offer stable mid-to-upper compensation with progression into program lead, people management, or regulatory writing leadership; exact figures vary by region and are not stated in the posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
–
Date found
2026-10-26
Intelligence details
Why this is worth applying to
Worth considering if you already have clinical trial documentation, ethics/consent, or regulatory writing exposure and want a structured CRO career path; clinicians without document or project management experience will likely find the senior bar steep.
Who should apply
Physicians, nurses, pharmacists, and IMGs with clinical research coordination, ethics committee, GCP, or regulatory/medical writing exposure who want to move into CRO-based document project management.
CV angle
Reframe real clinical experience around documentation and coordination: protocol and consent-related work, ethics/IRB submissions, GCP training, multi-site or cross-functional coordination, version control and QC of clinical documents, and timeline tracking — quantify sites, documents, or study volumes where truthful.
Skills to highlight
- Informed consent form development and review
- ICH-GCP and regulatory compliance
- Clinical trial documentation lifecycle
- Project and timeline management
- Cross-functional and site stakeholder communication
- Quality control and consistency review
- Vendor and translation coordination
- Medical writing and editing
Role summary
A senior project management role within Thermo Fisher's clinical research business, overseeing the drafting, review, and delivery of informed consent forms and related medical writing deliverables for clinical trials, coordinating writers, sites, sponsors, and internal teams against regulatory and study timelines.
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