Takeda
Agawam, MA, USA
Job Description
OBJECTIVES:
Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business units and affiliates.
Contributes to and implements the engagement strategy among R&D, Business Units and affiliates and Quality to ensure a global framework and robust quality systems are in place for the transition of R&D pipeline to the commercial space.
Drives a fit‑for‑use global Quality framework that elevates the capabilities in the business units and the affiliate and enables them to deliver their clinical research and pharmacovigilance‑related regulated activities with high compliance and agility.
Establish and maintain relationships with key stakeholders outside R&D such as the commercial Business Units, affiliates, Global Medical, Commercial Quality, etc., supporting post‑authorization strategies through thought partnership and linking R&D SMEs and experts, as needed.
How will...