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associated regulatory interactions Real-world evidence generation and analysis to identify unmet needs and inform comparative effectiveness, global epidemiology (including race, ethnicity, age, sex) to support
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are also expected to drive a paradigm shift in medical device security regulation, moving evaluation away from individual components and toward system-level thinking across vast networks of interacting
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, and impact of a Medical Affairs department, both within the organization and in its interactions with the broader healthcare community. During the fellowship, participants will work on diverse projects
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fellows with a comprehensive introduction to the structure, responsibilities, and impact of a Medical Affairs department, both within the organization and in its interactions with the broader healthcare
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well as experience partner interactions and engage in vendor oversight. The fellowship training will enable them to collaborate effectively with colleagues across various disciplines which is essential to both
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fellows with a comprehensive introduction to the structure, responsibilities, and impact of a Medical Affairs department, both within the organization and in its interactions with the broader healthcare
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development and post-marketing research, HCP and patient interactions, scientific publications, field materials, sponsorships, grants. Fellow activity will often involve working cross-functionally with teams
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interactions with regulatory bodies. Qualifications Doctor of Pharmacy degree from an ACPE-accredited institution Eligible for pharmacist licensure in the State of Massachusetts Excellent oral and written
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Affairs, Commercial, and Nonclinical groups to help operationalize regulatory strategy. Support regulatory interactions with regulatory bodies including preparation of meeting requests and briefing
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years of the fellowship program, mentorship opportunities and one on one interactions with Global Medical Affairs leaders will be available. Upon completion of the program, fellows will have both broad