Associate Director

5 days ago

London, Greater London, United Kingdom GlaxoSmithKline Full time
Job Title: Associate Director

GlaxoSmithKline is seeking a highly skilled Associate Director to join our team. As a key member of our organization, you will be responsible for providing scientific expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting.

Key Responsibilities:
  1. Regulatory Reporting: Produce regulatory periodic reports and associated documentation globally according to the agreed process and timelines, and advise on content of regulatory periodic reports.
  2. Safety Contribution: SERM safety contribution to global regulatory submissions, including RMPs.
  3. Risk Management: Ensure risk-reduction strategies are implemented appropriately in clinical study protocols and/or product labelling.
  4. Pharmacovigilance: Make recommendations for the further characterization, management, and communication of safety risks.
  5. Team Collaboration: Work collaboratively with a team of physicians and scientists supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally.

As an Associate Director at GlaxoSmithKline, you will have the opportunity to work on a wide range of projects and contribute to the development of our organization. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply for this exciting opportunity.

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