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Senior Director of Medical Writing
2 months ago
We are seeking a highly motivated Senior Director of Medical Writing to join our leadership team at iPowerPartner. As a key member of our team, you will be responsible for planning, developing, and writing clinical documents to support medical and regulatory activities across our product portfolio.
Key Responsibilities- Lead planning and authoring of complex clinical and regulatory documents.
- Guide medical writing and project teams during the planning and authoring stages.
- Drive strategic medical writing initiatives and processes.
- Contribute to/lead Medical Writing digitalization efforts.
- Lead development, review, and improvement of departmental processes.
- Coordinate with the Technical Document Manager and Document Quality Control groups.
- May oversee medical writing vendors/CROs.
- Proactively engage in department activities and mentor junior writers.
- Provide input to the overall strategy and development of the Medical Writing department.
- At least BA/BS degree in Life Sciences
- 13+ years of medical or scientific writing experience in the pharmaceutical industry.
- Oncology and immunology experience is a must
- Extensive experience in writing various clinical documents and regulatory filings.
- Expert understanding of regulatory requirements, drug development processes, and Good Clinical Practice.
- Proficiency in document content preparation and interpreting complex data presentations.
- Proficiency in relevant software.
- Market competitive compensation package including performance-based annual bonus scheme
- Company shares (generous welcome grant and performance-based annual equity plan)
- In-house and external learning and development opportunities
- Fantastic benefits program and keep improving
- Opportunity to work with a dynamic team of collaborative, supportive, inclusive, and fun professionals whose mission is clear: Cancer has no borders and neither do we.
