A global pharmaceuticals company is seeking an experienced Global Program Regulatory Associate Director in London. The ideal candidate will direct regulatory document development and submission, ensuring compliance and timely approvals. Responsibilities include implementing regulatory strategies and managing health authority interactions. Candidates must possess a relevant degree and significant experience in regulatory affairs. A strong track record in project management, excellent negotiation skills, and fluency in English are essential. The role offers hybrid working options. #J-18808-Ljbffr
Contact Detail:
Novartis Recruiting Team