Head of Regulatory Documentation
6 days ago
About the Role
We are seeking a highly experienced Senior Manager, Medical Writing to join our team at Proclinical Staffing. This role will involve creating and maintaining clinical documents, ensuring compliance with regulations and standards.
Key Responsibilities
- Develop high-quality writing deliverables on time and within budget.
- Plan, write, edit, and format key clinical documents independently, demonstrating expertise in regulatory submissions.
- Manage the review and finalization process for documents, ensuring seamless collaboration with project teams.
- Represent Medical Writing on project teams and collaborate with the Director of Medical Writing to drive business objectives.
- Work effectively with various internal and external stakeholders, fostering strong relationships and communication.
- Serve as a subject matter expert for clinical document production, staying up-to-date with industry developments and best practices.
- Contribute to the development and maintenance of SOPs and templates, ensuring consistency and efficiency across the organization.
Salary and Benefits
The estimated salary for this position is $110,000 - $140,000 per year, depending on experience and qualifications. We offer a comprehensive benefits package, including health insurance, retirement plans, and paid time off.
How to Apply
If you are interested in this exciting opportunity, please submit your resume and cover letter through our website. We look forward to reviewing your application and discussing how you can contribute to our team's success.
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