Senior Medical Writer shaping key clinical and regulatory documents at Thermo Fisher Scientific. Collaborating with teams to drive strategy, quality, and execution of early - phase programs.
About the role
- Lead Medical Writer responsible for clinical study documents at Fortrea. Collaborating with writers and ensuring high-quality delivery for various studies.
Responsibilities
- Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs)
- Provides support to more experienced writers with the preparation of clinical study protocols and CSRs
- Responsible for preparation and review of clinical documents such as patient safety narratives and CSR appendices
- Ensure timely delivery of high-quality documents to internal customers and Sponsors
- Foster excellent working relationships with all clients, both internal and external
Requirements
- First degree in life sciences (or equivalent)
- Advanced degree (e.g., PhD or Masters) preferred
- Typically, minimum 1 years medical writing experience or 2 years professionally-related experience
- Excellent command of written and spoken English
- In-depth knowledge of MS Word
- Good organizational and time management ability
- Excellent interpersonal skills
- Scientific or Clinical research experience desirable
- Good scientific writing skills
- Understanding of medical, pharmacokinetic, and statistical principles
Benefits
- EEO & Accommodations
- Professional development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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