Onsite Medical Writer: CSR & Regulatory Submissions

A biotechnology firm is looking for an experienced Medical Writer to produce critical documentation across clinical development and regulatory activities. Candidates should have over 10 years of experience in medical writing with a strong background in statistical analysis and regulatory submissions. This role demands onsite collaboration in San Diego for two weeks each month. The company offers a supportive environment with benefits like medical and vision insurance, a 401(k), and disability coverage. #J-18808-Ljbffr