Regulatory Affairs Internship at GSK in Canada
An exciting Regulatory Affairs Internship at GSK Careers in Canada for students interested in gaining hands-on experience in regulatory documentation, clinical trial support, and healthcare administration. This Summer 2026 internship provides an opportunity to work closely with the Regulatory Affairs team, support document management processes, and learn how regulatory systems operate within a global biopharmaceutical company.
About the Company:
GSK is a global biopharmaceutical company focused on uniting science, technology, and talent to get ahead of disease together. The company develops innovative medicines and vaccines to improve health outcomes for people worldwide.
GSK focuses on key therapeutic areas including respiratory diseases, immunology and inflammation, oncology, HIV, and infectious diseases. With a mission to positively impact 2.5 billion people by the end of the decade, GSK continues to invest in scientific innovation, research, and healthcare solutions that benefit patients around the world.
Internship Details:
- Role: Regulatory Affairs Intern
- Location: Canada
- Type: Internship
- Work Duration: 4 Months (Summer 2026)
- Work Schedule: Full Time
- Salary Range: CAD $31,980 – CAD $79,950 annually (depending on education and experience)
Key Responsibilities:
- Support document management activities, including bookmarking Common Product Information Documents (CPIDs) in this Refulatory Affairs Internship in Canada.
- Create and maintain regulatory lifecycle management tables.
- Prepare and process administrative forms related to clinical trial activities in this Regulatory Affairs Internship at GSK Careers.
- Provide general administrative and operational support to the Regulatory Affairs team in this Summer Internship.
- Assist with documentation, organization, and regulatory correspondence management.
- Support various ad hoc administrative tasks within the regulatory department in this Regulatory Affairs Intern role.
Educational Requirements for this Internship:
Candidates must meet the following academic requirements:
- Currently enrolled in a post-secondary program such as Life Sciences, Health Sciences, Biotechnology, or related fields
- Must be returning to post-secondary studies in Fall 2026.
Skills Required:
- Strong organizational and documentation management skills.
- Close attention to detail.
- Ability to manage multiple tasks and meet deadlines.
- Effective written and verbal communication skills.
- Proficiency in Microsoft Office applications, particularly Word and Excel.
- Interest in regulatory affairs, healthcare, or clinical research.
Benefits of the Regulatory Affairs Internship:
This internship provides valuable learning and career advantages:
- Hands-on experience in regulatory administrative processes within the healthcare industry.
- Exposure to Health Canada regulatory correspondence and documentation standards.
- Opportunity to develop skills in regulatory lifecycle management and clinical trial support.
- Mentorship and collaboration with experienced regulatory affairs professionals.
- Experience working with a leading global biopharmaceutical company focused on improving patient health.
