Job Summary
A company is looking for an Associate Director, Program Management.
Key Responsibilities
- Develop and execute regulatory plans, timelines, and budgets for Atacicept
- Act as a liaison between Regulatory and Development functions, managing updates across workstreams
- Provide support for regulatory submissions, including timeline development and status reporting
Required Qualifications
- BA/BS degree with 8+ years of biotechnology industry experience
- In-depth knowledge of biopharmaceutical industry and biologic development preferred
- Experience in regulatory and global filings required
- Demonstrated people management skills, specifically managing other program managers
- Proficient in Microsoft Office and experience in Smartsheet preferred
Comments