Director, Medical Writing

About the role

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Responsibilities

• Positively contributes to departmental growth by working cross-functionally on the continuous development/improvement of medical writing/quality control processes to ensure that work is high quality, uniform, complete, managed appropriately, and meets ProPharma and client standards.
• Leads medical writing business development efforts (capabilities meetings, bids/contracts, proposal development, budget review, and bid defenses; travel may be required).
• Organizes and leads departmental initiatives (e.g., process improvement, lunch and learns, etc.).
• In collaboration with other medical writing leadership, defines and manages medical writing and quality control resource needs, and communicates with recruiting and business development in a timely and effective manner.
• Ensures appropriate communication on project- and program-related matters with other medical writing leadership, internal functional area heads, and internal resources/consultants.