Role: Regulatory & Medical Affairs - Medical Writer Location: Lawrence Township, NJ Duration: 12+ months W23 Contract Job Description: Oncology Medical Writer

…support. Safeguard patient safety. Provide expert medical support to Regulatory Affairs , Communications, Legal, and Quality/Risk Management/ Product

Consultant, Director of Clinical/Medical Affairs , Medical Technology Summary Our client, a clinical stage medical technology company, has engaged GForce Life

…alignment where complex cross-functional interfaces exist such as with development, regulatory affairs , medical, operations, clinical, and commercial functions.

…writing, IRB activities, infectious diseases, working with HIV patients, and/or regulatory affairs are highly desirable. Technical Resources International is

…collaboration with Commercial organization, Clinical Research and Development, HEOR and Regulatory Affairs . Key Responsibilities Develops and implements Medical

…resource allocation in close partnership with the cross-functional and regional partners in Regulatory and Medical and (Pre-) Clinical Affairs , as well as

…(DCI) and other appropriate departments and/or institutions ensuring compliance with regulatory affairs and requirements of relevance to the Institutional

…medical/scientific strategic and operational input into core medical affairs activities such as: health-care professional/provider interactions; generation of

…with key functions, including Digital Health Platform teams, PD, GPS, Medical Affairs , Regulatory , Informatics, Commercial and other Roche Affiliates (Flatiron,