Job Summary
A company is looking for a Principal Medical Writer to provide high-quality medical and scientific writing in a remote role dedicated to a client in the FSP space.
Key Responsibilities
- Research, write, and edit clinical study reports and study protocols, summarizing data from clinical studies
- Serve as the primary author for complex clinical and scientific documents, providing senior-level reviews and mentorship for other writers
- Ensure compliance with quality processes, develop best practices, and represent the department in project meetings
Required Qualifications
- Bachelor's degree in a scientific discipline; advanced degree preferred
- 8+ years of relevant experience in managing complex medical writing projects
- Experience in the pharmaceutical/CRO industry preferred
- Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous
- Significant knowledge of global document development guidelines and in-depth knowledge in specialty areas
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