Senior Medical Writer — Regulatory CSR/Protocol Lead

A leading biopharmaceutical solutions organization in New Jersey is seeking a Senior Medical Writer to manage and complete regulatory documents. Responsibilities include writing clinical study protocols, ensuring adherence to regulatory standards, and mentoring junior writers. The ideal candidate will have over 5 years of experience in medical writing and excellent communication skills. This position offers competitive salary ranging from $80,600 to $145,000, along with a comprehensive benefits package including health insurance and flexible PTO.
#J-18808-Ljbffr