Associate Director, Medical Writing
Summit Therapeutics Inc.
Responsibilities Prepare, edit, and finalize clinical/regulatory documents including protocols, CSRs, and Investigator's Brochures Interact with cross-functional contributors to acquire necessary input Manage document review processes and timelines Facilitate comment resolution and adjudication with project teams Participate in the refinement of medical writing processes and SOPs Requirements BA/BS degree in a scientific field (PhD, PharmD, or MS preferred) 8+ years of regulatory medical writing experience in the pharmaceutical industry Experience writing clinical study protocols, CSRs, and IND/NDA submissions Knowledge of oncology disease areas preferred Proficiency in MS Office, Adobe Acrobat, and electronic document management systems Ability to manage multiple projects simultaneously with minimal direction About the Company Summit Therapeutics Inc. is a biopharmaceutical oncology company focused on improving quality of life and resolving serious unmet medical needs through clinical studies in oncology. #J-18808-Ljbffr Summit Therapeutics Inc.
Vacancy posted 6 days ago
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