Future Talent Program – Global Regulatory Affairs – Oncology Co‑op

About the role

The Future Talent Program offers a 4‑6 month co‑op in Global Regulatory Affairs focusing on oncology drug development. You will work on one or more regulatory projects under a mentor, gaining hands‑on experience in the drug development process.

Key responsibilities

• Support regulatory affairs activities for oncology clinical development, including document preparation and submission tracking.
• Collaborate with cross‑functional teams to gather scientific data and ensure compliance with regulatory guidelines.
• Observe and participate in regulatory strategy discussions and project meetings.

Required profile

• Enrolled in a Bachelor’s, Master’s or PhD program in biological sciences, life sciences, pharmacology, medicine or a related field.
• Completed at least three years of study and participating in a university co‑op program.
• Strong academic performance, communication and teamwork skills, and ability to work independently.

Required skills

• Proficiency with Microsoft Office applications.
• Ability to write scientific documents and communicate technical information clearly.
• Comfortable using Windows‑based operating systems, spreadsheets and basic database tools.