
Program Manager – Regulatory Medical Writing
Thermo Fisher Scientific
full-time
Posted on:
Location Type: Remote
Location: North Carolina • United States
Visit company websiteExplore more
About the role
- Lead client programs with high visibility among internal and client teams
- Manage client relationships and identify and resolve client management issues
- Ensure the timely delivery and the quality of multiple program documents
- Develop, monitor, and adapt project plans, client and program-specific processes, timelines, and budgets/forecasting for programs
- Serve as subject matter expert for assigned programs
Requirements
- Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years)
- Experience in managing and directing complex medical writing projects required
- Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous
- Solid program management skills to include budgeting, forecasting and resource management
- Extensive knowledge of global, regional, national and other document development guidelines
- In-depth knowledge in one or more specialty areas such as preclinical, therapeutic, regulatory, submissions, communications, etc.
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
program managementmedical writingbudgetingforecastingresource managementproject planningdocument development
Soft Skills
client relationship managementproblem resolutiontimely deliveryquality assuranceadaptability
Certifications
AMWAEMWARAC