Clinical Data Lead

Are you ready to contribute to high-impact clinical data management activities that help drive the development of innovative medicines and improve patient outcomes? As a focused biopharma company, we discover, develop and deliver medicines and vaccines to create value for patients and shareholders.

This is a hybrid role based out of Mississauga, requiring 23 business days per week in the office, and reports directly to the Director of Data Management.

Internal candidates are encouraged to submit by Friday, June 5, 2026.

• Electronic Case Report Forms (eCRFs), vendor data, and other clinical outcome assessments
• Defining and executing the Data Management strategy, including data ingestion, cleaning, and reconciliation.
• Managing interim and final cleaned database locks.
• Archival of all Data Management documents within the eTMF.
• Archival of study databases and provision of clinical data to study sites.
• Leading day-to-day DS&M operational study activities for in-house studies and serving as the single point of contact for all Data Management matters.
• Conducting and documenting sponsor oversight of end-to-end FSP study activities and ensuring protocol training for FSP resources supporting the study.
• Supporting oversight activities for Full-Service Outsourced (FSO) studies where applicable.
• Providing Data Management operational input into study design, protocols, study planning, study documents, and study risk registers.
• Providing reports, status updates, feedback, and guidance to key study stakeholders on study progress.
• Creating or reviewing study-level timelines for Data Management deliverables and ensuring adherence to timelines.
• Acting as the first point of escalation for Data Management study issues and ensuring compliance with GSK SOPs and regulatory guidelines.

• Bachelors degree in a scientific, health-related, or business discipline.
• Experience with Clinical Data Management processes, standards, and clinical systems.
• Proficiency in Microsoft Excel and validation methodologies.
• Basic knowledge of PL/SQL and SAS is considered an asset.
• Understanding of data flow processes and database architecture concepts.
• Good understanding of regulatory requirements and industry standards, including ICH-GCP, 21 CFR Part 11, and CDISC.
• Comprehensive understanding of the clinical drug and vaccine development lifecycle.
• Knowledge of medical terminology, anatomy, and physiology.
• Strong project management and organizational skills.
• Familiarity with EDC platforms such as InForm, Rave, Veeva, Oracle Clinical (OC), e-Diaries, and e-Source systems is considered an asset.

• Strong organizational, prioritization, and time management skills with keen attention to detail.
• Excellent interpersonal, teamwork, and communication skills with the ability to work effectively in a global environment.
• Adaptable and results-oriented professional with a problem-solving mindset and ability to learn quickly.

The annual compensation for this role is CAD
100,000 to CAD
150,000, determined based on experience, qualifications, and internal equity.

GSK is an Equal Chance Employer.