Medical Doctor Job at GSK in Europe | Apply now
A Medical Doctor job opportunity is available at GSK for the role of SERM Associate Medical Director in Warsaw, Poland. This role provides medical leadership and expertise in safety evaluation and risk management within oncology clinical programs. Professionals seeking medical jobs in Poland, medical jobs in Europe, or global careers in leading healthcare organizations like jobs in GSK can explore this opportunity to contribute to patient safety, clinical research, and drug development.
Job Details:
- Job Title: SERM Associate Medical Director
- Location: Warsaw, Poland
- Department: Medical and Clinical
- Job ID: 434714
- Site Name: Warsaw
About the Company:
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
Job Description:
The SERM Associate Medical Director provides medical leadership and subject-matter expertise to Safety Evaluation & Risk Management (SERM) activities across assigned clinical programs within oncology. The role integrates clinical/medical insight with safety and risk assessment processes to identify patient- and study-related risks, shape mitigation strategies, and ensure regulatory and ethical compliance.
This Medical Doctor job plays an important role in supporting patient safety and drug development within oncology clinical research programs at GSK.
Qualifications:
- Medical Doctor (physician) preferred; equivalent qualifications (e.g.,dentist) accepted with relevant pharmacovigilance (PV) experience.
- Postgraduate qualifications in medical or scientific fields desirable.
- Substantial expertise in pharmacovigilance or drug development across clinical and post-marketing settings.
- Knowledge of international PV requirements (ICH, GVP, CIOMS) and drug approval processes.
- Experience working in large matrix organizations.
Key Responsibilities:
- Provide medical oversight and clinical input to SERM risk assessments, safety monitoring and mitigations, and overall evaluation of benefit/risk.
- Interpret clinical data and lead assessment of safety signals.
- Collaborate with team members within Safety, Clinical Development, Regulatory Affairs, and other functions to develop effective safety strategies and communications.
- Contribute to design and review of protocols, risk assessment tools, and medical sections of safety risk documentation.
- Draft, review, and approve medical content for INDSRs, risk registers, and regulatory submissions.
- Participate in cross‑functional governance forums and advise senior leadership on medical implications of safety/risk scenarios.
- Support training and capability building for colleagues on clinical aspects of safety-related risks and mitigation strategies.
- Maintain awareness of applicable regulations, guidance, and industry best practices.
