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2027 Future Talent Program – Global Regulatory Affairs - Oncology – Co-op

Merck
September 07, 2026
Full-time
Remote friendly (Rahway, NJ)
Worldwide
Clinical Research and Development
Role: Co-op student in Regulatory Affairs focusing on oncology drug development, providing observational and hands-on experience within the drug development process and regulatory submissions. Responsibilities: support regulatory projects in oncology, collaborate with multidisciplinary teams, and develop understanding of regulatory strategies. Requirements: enrolled in a Bachelor's (3 years completed) or higher in biological sciences or related field; ability to work full-time onsite (hybrid) for 4-6 months; strong Microsoft Office and scientific communication skills. Preferred: current enrollment in MS or PhD programs, interest in pharmaceutical industry, proactive, with good critical thinking, teamwork, and time management skills. HighValue: oncology therapeutic area, regulatory affairs, clinical development process, regulatory submissions, cross-functional collaboration, observational and project involvement during drug development lifecycle. WorkSetup: hybrid onsite, no travel required.