Lead Senior Medical Writer for Olema Oncology's oncology portfolio, developing and delivering high-quality scientific and regulatory documents, and leading cross-functional teams to translate complex data into clear content.
Requirements
- Bachelor's degree in life sciences, pharmacy, or related field
- Minimum 7+ years of medical or regulatory writing experience
- Strong project management skills
- Excellent scientific writing and editing skills
- Familiarity with regulatory writing standards (e.g., ICH E3/E6, GPP)
- Oncology preferred
- Veeva RIM experience is a plus
- Prior experience in clinical-trial documentation for oncology preferred
- Ability to work independently and collaboratively
- Detail-oriented and organized
- Proficiency with standard technical and document-management tools
- Strong verbal communication skills
Benefits
- Competitive compensation and benefits package
- Equity
- Bonus
- Paid Time Off
- 401k Matching
- Retirement Plan
- Flexible and friendly work environment