Director, Medical Review Scientist - CTMRT

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Site Name: Warsaw, Poland or Mississauga, Canada

Posted Date: Oct 27 2025

At GSK, we have bold ambitions for patients, aiming to positively impact the health of billions of people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting‑edge technology to transform lives.

Position Summary

GSK is expanding the Oncology Clinical Development organization and is seeking experienced professionals to join our journey. The Clinical Trial Medical Review Team (CTMRT) is a specialized function within oncology that integrates Medical Review Scientists with study teams to deliver a complete, robust, and medically accurate data package.

As a Director, Medical Review Scientist – CTMRT you will perform medical review activities across multiple oncology studies, mentor Associate Directors, and collaborate with cross‑functional teams to ensure data integrity.

Responsibilities

• Ensure the medical consistency and robustness of clinical data that cannot be processed by computerized means, through iterative, in‑stream, standardized data review.
• Review and contribute to study‑related documents such as protocols, medical monitoring plans, statistical analysis plans, data management plans, eCRFs, and risk‑based monitoring plans.
• Develop a Medical Review Plan (MRP) during study set‑up, detailing scope, timelines, and review activities.
• Execute medical review during the data collection phase as defined in the MRP.
• Collaborate with the Centralized Monitoring team to identify key study risks based on iterative medical review.
• Support medical coders to ensure consistency and accuracy of adverse events, medical history, and concomitant medication coding.
• Review statistical program outputs for inconsistencies and areas needing addressing by the CTMRT.
• Address medical queries, analyze data inconsistencies, and develop site training materials as needed.
• Participate in weekly study team meetings and update on medical review status and trend analysis.
• Identify program or data risks and implement mitigation strategies in collaboration with the Clinical Study Team.
• Ensure eCRFs and eCRF completion guidelines accurately reflect the patient population and protocol scope.
• Collaborate closely with Study Physicians, Clinical Scientists, and Patient Safety to review complex medical questions and concepts.

Basic Qualifications

• Bachelor’s in Life Sciences with 8+ years of industry experience and 3+ years in oncology, or equivalent clinical experience.
• Experience in data review/interpretation, study design, and the clinical development process.
• Proficiency with electronic data capture (EDC) systems, query management, and Medical Review tools.
• Knowledge of regulatory requirements, including GCP principles.
• Excellent written and verbal communication skills with strong presentation abilities.
• Ability to work productively in a fast‑paced, collaborative environment with a positive attitude.

Preferred Qualifications

• Advanced degree (Master’s, PhD, PharmD) or 10+ years of experience.
• Advanced understanding of clinical development and/or marketed support to recommend, influence, and implement process improvements.

Work Location

This role is based in Warsaw, Poland or Mississauga, Canada and offers a hybrid working model.

Equal Opportunity Employer

GSK is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), age, disability, or other protected characteristics. GSK is also a required source of the General Availability that constitutes the CDC evidence of the donation or random testing addresses problem increases among appetite for large kill.

Please provide your resume and a cover letter.