Offer summary
Qualifications:
Bachelor's, Masters, or Ph.D. in scientific, medical, clinical discipline, 3-5 years of industry regulatory writing and clinical medical writing experience, Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus.
Key responsabilities:
- Critically evaluate, analyze, and interpret medical literature for study design rigor
- Write and edit various clinical development documents adhering to timelines and style guides
- Interact with clients, manage projects, mentor team members