Fellowship in Industry Program — Partner Therapeutics

This unique two-year fellowship program is a 50/50 split of medical affairs and clinical development with additional exposure to regulatory science in the first
year. The program will help prepare the fellow to become a well-rounded industry leader. This is one of the few programs in the country that balances the
fellow’s long-term goals with institutional priorities.

Activities at Partner Therapeutics

The fellow will function as a clinical trial management associate and support clinical trial managers and clinical program managers on the following activities:

Medical Affairs

• Develop and maintain scientific expertise in therapeutic area(s) relevant to the company’s portfolio.
• Support the creation and review of scientific content, including slide decks, medical information letters, FAQs and standard response documents.
• Participate in medical review of promotional and non-promotional materials to ensure scientific accuracy and regulatory compliance.
• Engage with cross-functional partners (regulatory, commercial, clinical operations) to provide medical and scientific insights.
• Respond to unsolicited medical information requests from health care professionals.
• Collaborate with field medical teams (MSLs) by preparing resources, training and supporting scientific exchange initiatives.
• Contribute to scientific congress planning and execution, including booth activities, medical information dissemination and competitive intelligence collection.
• Assist in generating real-world evidence and publications, including abstracts, posters and manuscripts.

Clinical Development

• Gain exposure to the design, implementation and management of clinical trials across multiple phases.
• Assist in drafting clinical study protocols, informed consent forms and case report forms.
• Contribute to safety monitoring, adverse event reporting and data review for ongoing studies.
• Support cross-functional study team meetings and clinical operations activities.
• Participate in interactions with clinical investigators, study sites and contract research organizations (CROs).
• Collaborate on data analysis, interpretation of study results and preparation of clinical study reports.
• Contribute to regulatory submissions and responses by providing clinical and scientific input.
• Monitor scientific and clinical landscapes to identify unmet medical needs and potential trial opportunities.

Fellowship Program Dates

The fellowship begins July 1, 2026 and ends June 30, 2028.