, Global Regulatory Lead (GRL) in Neurology supports neurology programs across all phases of clinical development. The..., from late research to post marketing. At the project level, the individual will lead the Global Regulatory Team (GRT...
Director, Global Regulatory Lead Oncology where you will be part of the global regulatory team. As Associate Director, Global... Regulatory Lead Oncology, you will define and lead global regulatory strategies for oncology programs, oversee major submissions...
Job Title: Associate Director, Global Scientific Communications Lead Location: Cambridge, MA 02142: Remote Duration...: 12 Months 8 AM to 4 PM Objectives/Purpose The Associate Director, Global Scientific Communications Lead is a key...
Job Description Summary The Regulatory Diagnostics Associate Director (RDAD) for Precision Diagnostics is responsible... adherence to regulatory requirements. The RD Associate Director will also provide regulatory support including tactical...
and modest costs. Description of Role Our Associate Director, Regulatory Affairs Reporting will be responsible for performing... Director, Regulatory Affairs, you will act as the regulatory lead on project teams, providing regulatory guidance and oversight...
, Massachusetts. The Position The purpose of the Associate Director, Regulatory Strategy role is to support the development... and implementation of innovative global regulatory strategies for preclinical and early clinical development products, as assigned...
-on Regulatory Affairs professional to contribute to the development strategy and lead in the planning, preparation, submission.... What you’ll be doing As a key member of the Nuvation Regulatory Affairs team, you will collaborate with a cross-functional team...
: Clinical Pharmacology Lead (Associate Director) Our Clinical Pharmacology Leads have key roles to play in influencing the...OVERVIEW: Exciting opportunity in Clinical Pharmacology! Our Clinical Pharmacology Team is looking for an Associate...
Job Title: Associate Director, Scientific Communications Lead (Hematology, Global Medical Affairs Oncology) Location... skills. The Associate Director, Scientific Communications Lead, develops and implements strategic publications...
Job Description General Summary: Vertex Pharmaceuticals is looking to hire an Associate Director, North America... that will enable them to lead through science. The individual must be a strong collaborator to work cross-functionally within the...
to meet both short- and long-term requirements. The Associate Director will be responsible for working with the commercial... for improvement. The Associate Director will use the dynamic capacity model to recommend scheduling strategies, future capacity needs...
Job Description General Summary: The Associate Director, GMP Operational Quality will provide leadership..., and data generated by external laboratories meet Vertex, global regulatory, and data integrity standards. Key Duties...
Job Description General Summary: The Associate Director, GMP Operational Quality is an advanced technical resource... continuity, support for global jurisdictional expansion, and high‑level combination product quality alignment. The incumbent...
Job Description The Associate Director is recognized as an expert in the principles and application of quality... of Commercial Release and serves as primary QA contact on cross-functional teams. The Associate Director manages and develops...
Associate Director, GCP Audit & Compliance provides strategic quality oversight to clinical, medical, and pharmacovigilance... suppliers across Takeda’s global network. You will lead the risk-based supplier audit program, drive compliance insights...
Job Description General Summary: Vertex Pharmaceuticals is seeking an Associate Director (AD) of Kidney Field... Training & Development to join the North America Commercial Field Training (NACFT) organization. Reporting to the Director...
not just supplying medicine; we're improving the standard of care for more patients around the world. The Associate Director.... This role will report into the Rare Emergency Medicine Head of Marketing. As Associate Director, Marketing...
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...