Job Title: Clinical Regulatory Writing Manager (Associate Director) Location: Boston, MA - Hybrid Introduction...: As a Clinical Regulatory Writing Manager (Associate Director), you will: Independently manage clinical regulatory writing...
Job Description General Summary: The Associate Director, Medical Writing Science manages the overall operations... for document development for regulatory filings and coordinates the clinical sections of more complex regulatory submissions...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 Duration: 12 Months Hybrid... role - Shift: 8 AM to 5 PM OBJECTIVES: Provides quality assurance oversight of the global clinical research programs...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 - Hybrid Duration: 12 Months... global clinical research programs in Oncology Business Unit (OBU) with the overall goal of inspection readiness. Serves...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 - Hybrid Duration: 12 Months... global clinical research programs in Oncology Business Unit (OBU) with the overall goal of inspection readiness. Serves...
Job Description: Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA Duration: 12...+ Months (Possible of Extension) Job Overview Provides quality assurance oversight of the global clinical research programs...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 Duration: 12 Months Hybrid... role - Shift: 8 AM to 5 PM OBJECTIVES: Provides quality assurance oversight of the global clinical research programs...
Job Description General Summary: Vertex Pharmaceuticals is looking to hire an Associate Director, North America..., Legal, Regulatory and Compliance teams). Key Duties and Responsibilities: Leading training activities primarily for the...