Seeking an experienced clinical medical writer for an 18 month contract. Must have a strong background in authoring Clinical Study Reports (CSRs), protocol design and amendments, and Investigator Brochures (IBs), including the integration of four new IBs. This role requires a self-starter who is highly motivated, able to work independently, communicate progress regularly (daily/weekly), and drive meaningful impact.
- 5+ years expereince in medical writing
- Must have experience in IND and NDA submission
- PhD or Masters required
- CRO, biotech or pharma background
- Oncology experience is required
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