, 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...
-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...
(Associate Director) - Global Manufacturing Science GMSci Drug Product (DP), you will provide technical expertise within the... projects associated with new product introductions and the life cycle management of existing products. You will lead regulatory...
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...
milestones. Summary Description: The Reg Nonclinical / Clinical Associate Director will lead, conceive, communicate...The Global Regulatory Affairs (GRA) is responsible for obtaining approval for new products and ensuring that approval...
integration while considering the evolving AI landscape. The Associate Director will also serve as the Consumer Digital lead...Job Description General Summary: Associate Director, Consumer Digital Marketing will be responsible for developing...
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...
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...
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...
Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 9893 Responsibilities The Associate Director... oversight on the clinical trial process to ensure continuous inspection readiness and compliance with Regulatory Authorities...
: As Associate Director, Clinical Science, you will work in a cross-functional clinical matrix team, fostering a collaborative... study design. Lead or co-author and review essential clinical and regulatory documentation as appropriate, including...