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Medical Director

2 months ago


London, Greater London, United Kingdom GlaxoSmithKline Full time
About the Role

We are seeking a highly skilled Medical Director to join our team in the Safety Evaluation and Risk Management department. As a key member of our team, you will be responsible for providing medical expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting.

Key Responsibilities
  • Provide medical expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting.
  • Ensure scientifically sound review and interpretation of data and management of safety issues, and escalate safety issues identified through the safety review process to senior management and safety governance as appropriate.
  • Focus on efficiency and effectiveness to meet the needs of our Patients and Regulatory Authorities.
  • Be part of 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.
What We Offer

We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We also embrace modern work practises, with our Performance with Choice programme offering a hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Requirements
  • Medical Doctor (physician)
  • Substantial experience in pharmacovigilance or drug development.
  • Pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing clinical development and/or post-marketing activities.
  • Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes.
  • Ability to function successfully in cross-functional groups.
Preferred Qualifications
  • Experience working in large matrix organizations.
  • Experience working globally in pharmacovigilance or drug development.
  • IT competencies.