Principal Medical Writer

A company is looking for a Principal Medical Writer (Regulatory MW).

Key Responsibilities

Lead the preparation of high-quality regulatory medical writing documents, ensuring compliance and accuracy

Serve as the primary author for clinical study reports, study protocols, and other complex documents

Provide training and mentorship to junior writers and assist in program management activities

Required Qualifications

Bachelor's degree in a scientific discipline; advanced degree preferred

8+ years of relevant experience in regulatory medical writing

Experience managing complex regulatory medical writing projects

Preferred experience in the pharmaceutical or CRO industry

Additional qualifications in medical writing (AMWA; EMWA; RAC) are advantageous