Regulatory Content Manager
3 days ago
**Key Responsibilities**
- Prepare clinical regulatory documents, including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures.
- Oversee and coordinate other writers and QC specialists assisting on documents under your responsibility.
- Ensure timely delivery of documents and manage project budgets.
- Work closely with clients and authors to coordinate review cycles, meetings, and project timelines.
**Requirements**
- At least 3 years of experience actively writing regulatory documents.
- Experience working as a lead writer on complex projects.
- Strong understanding of clinical regulatory documents and industry standards.
- Excellent communication and interpersonal skills.
- Ability to work under tight deadlines and prioritize tasks effectively.
**Compensation**
The estimated salary for this position is $120,000 - $150,000 per year, depending on experience.
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