SERM Associate Scientific Director

GSK · London, New Oxford Street · PLN 318,000 to PLN 530,000 · hybrid Join GSK as a SERM Associate Scientific Director in the United Kingdom and use your medical and scientific expertise to support patient safety worldwide. You will work closely with cross-functional teams to evaluate safety data and manage risks across key products in clinical development and the post-marketing setting. Your clear, thoughtful insights will help shape decision-making and improve outcomes for patients and healthcare professionals. Responsibilities: Lead or contribute signal detection and evaluation activities for assigned products, applying strong scientific judgment. Prepare and review global regulatory reports and risk management plans, ensuring accuracy and timely delivery. Support safety governance meetings and collaborative safety review teams for clinical and post-marketing safety oversight. Contribute to the design and implementation of risk-reduction strategies in clinical protocols and product information. Build and maintain effective relationships across teams, providing clear communication and mentoring colleagues where appropriate. Participate in process improvements to enhance compliance, quality, and efficiency within safety evaluation activities. Basic Qualifications: A degree in Health Sciences or Healthcare Professional qualification (for example, BSc, MSc, PhD, RN, NP, PharmD). Practical experience in pharmacovigilance focusing on safety evaluation and risk management during clinical development and post-marketing phases. Understanding of international pharmacovigilance guidelines and drug development and approval processes. Experience working effectively in cross-functional, matrix teams. Strong scientific writing skills with the ability to prepare detailed safety evaluations and regulatory documents. Ability to manage multiple tasks with attention to detail and deliver high-quality results on time. Preferred Qualifications: Advanced degree (e.g., PhD, MD, or equivalent). Previous experience working in large, global pharmaceutical organizations. Familiarity with early clinical development safety activities. Experience contributing to safety governance and regulatory inspections or audits. Knowledge of relevant safety databases and data visualisation tools. Comfortable working in a hybrid model that combines remote and on-site work.