Job Summary
A clinical research firm has a current position open for a Remote Senior Principal Regulatory Medical Writer.
Core Responsibilities Include:
- Independently writing and formatting clinical and regulatory documents
- Project managing assignments
- Reviewing and approving clinical and regulatory documents
Must meet the following requirements for consideration:
- Bachelor's degree, or international equivalent
- 4-10 years of experience in medical/technical writing
- Expert in literature search techniques
- Depth of industry and drug development knowledge
- Strong knowledge and experience with Common Technical Document templates
- Superior working knowledge of software programs in Windows environment