Global Clinical Development Graduate Program, Canada, 2025
Company
GSK
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get ahead together. With over 300 years of innovation, we’re a science-led global healthcare company that discovers, develops and manufactures innovative medicines and vaccines. Join us and help millions of people do more, feel better, live longer.
Location
Mississauga
Duties
Manage study execution of trial(s) from start-up through close-out in accordance with study budget and timelines with the focus on setting up, maintaining and ensuring completeness of internal systems/databases/tracking tools and project plans
Work in collaboration with the SDL to provide end to end operational and administrative support for study delivery activities
Monitor study conduct and progress, identify, resolve and escalate risks/issues which may impact delivery of the study to the necessary quality, timeline and budget objectives
Interact with other study team members across different functions to ensure all issues, risks and successes with study delivery are reviewed and/or shared as they occur
Support Clinical Team in quality and data oversight to ensure inspection/audit readiness, including oversight of eTMF completeness
Facilitate and maintain interactions and meetings with internal and external vendors to ensure the successful delivery of assigned studies
Set up and maintenance of clinical trial management systems and tracking tools
Prepare and update of study documents and study plans
Learn about the drug development process
Gain broad experience across the field of clinical research and variety of therapeutic areas
Learn to manage projects and prioritize tasks
Requirements
Education required: BS degree from an accredited college/university, preferably in Sciences/Pharmacy. Graduation by August 2025.
Language requirement: Written and spoken fluency in English
Other requirements: Willingness to be geographically mobile (domestic) throughout rotations
Start Date
2025-09-01
Hours
+35
Contact
Name
Mackenzie Day
Display Name
Mackenzie Day
Title
HR
Job Posting Link
Display Date
2024-10-10
Expiry Date
2024-12-02
