Program Manager – Regulatory Medical Writing
Thermo Fisher Scientific
full-time
Posted on:
Location Type: Remote
Location: North Carolina • United States
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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
program managementmedical writingbudgetingforecastingresource managementproject planningdocument development
Soft skills
client relationship managementproblem resolutiontimely deliveryquality assuranceadaptability
Certifications
AMWAEMWARAC