Job Summary
A company is looking for a Senior Medical Writer (Remote).
Key Responsibilities
- Evaluate and analyze medical literature to support study design and scientific rigor
- Write and edit various clinical development documents and maintain timelines for assignments
- Mentor junior medical writers and manage project communication with clients
Required Qualifications
- Minimum of 3-5 years of regulatory and clinical medical writing experience in the pharmaceutical industry
- Bachelor's, Master's, or Ph.D. in a scientific or medical discipline
- Experience as a lead author on clinical study protocols
- Proficiency in MS Word, Excel, and PowerPoint
- Strong understanding of federal regulations and Good Clinical Practices
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