- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and strategic insights at the study team level. The Associate Director of Regulatory Writing … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small ... medical devicesExperience with FAIR principles and other standardsExperience writing and maintaining process documentation#eligibleforERPCurrent Employees apply HERE Current… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward ... portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team… more
- Merck & Co. (Rahway, NJ)
- …reputation while ensuring effective internal and external stakeholder engagement. The Executive Director will report to the Associate Vice President, Human ... Job DescriptionThe Executive Director , our Company's Manufacturing Division Communications, is responsible for leading communications for the company's worldwide… more
- Novo Nordisk (Lexington, MA)
- …The Position The Associate Director is an expert in medical writing and performs work independently with minimal-to-no supervision. The Associate ... input into development plans, study designs, and regulatory submissions. Relationships The Associate Director , Medical Writing (ADMW) reports to a … more
- Vera Therapeutics (Brisbane, CA)
- Job Title: Associate Director , Medical Writing Location: Brisbane, CA About Us: Vera Therapeutics (Nasdaq: VERA), is a late clinical-stage biotechnology ... from immunological diseases. Position Summary: Reporting to the Senior Director , Medical Writing , the Associate Director , Medical Writing… more
- J&J Family of Companies (Spring House, PA)
- We are recruiting for an Associate Director to join the Regulatory Medical Writing team to support the Oncology therapeutic area. The position may be ... our team? Then please read further! Key Responsibilities This position will lead medical writing (MW) activities in the Hematologic Malignancies disease area,… more
- Gilead Sciences, Inc. (New Bedford, MA)
- …Join Gilead and help create possible, together. **Job Description** Job Description Medical Writing acts as a strategic partner across drug discovery, ... development, and commercial teams. Medical Writing participates in cross-functional drug discovery,... writer to join our dynamic team at the Associate Director level. You will author a… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …as other research areas centered around rare diseases and immune disorders. **Summary** The Associate Director of Regulatory Writing is a key role ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and strategic insights at the study team level. The Associate Director of Regulatory Writing … more
