Clinical Data Lead - Mississauga, ON

GSK•Mississauga, ON

4d•CA$100,000 - CA$150,000•Hybrid

About The Position

GSK is looking to hire a Clinical Data Lead to join our Data Sciences & Management (DS&M) Team. This is a hybrid role based out of Mississauga, requiring 2–3 business days per week in the office, and reports directly to the Director of Data Management. As a Clinical Data Lead, you will be responsible for leading end-to-end clinical data management activities for one or more clinical studies, ensuring high-quality data delivery, regulatory compliance, and operational excellence. You will partner closely with clinical operations, biostatistics, programming, medical writing, and external vendors to support timely study execution and database delivery. Your ability to manage multiple priorities, communicate effectively, and collaborate across global teams will be critical to success. You will also support process improvements, vendor oversight, and mentoring initiatives while contributing to GSK’s mission to help patients do more, feel better, and live longer.

Requirements

Bachelor’s 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

Nice To Haves

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

Responsibilities

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