Proclinical is seeking an Associate Director of Regulatory Affairs to join a dynamic team in the oncology and pharmaceutical sector. This remote, contract-based position requires expertise in regulatory affairs and strong cross-functional collaboration across global development programs.
The role focuses on leading global regulatory strategies and submissions, managing health authority engagement, and guiding regulatory designations such as Orphan Drug or Fast Track as part of development plans.
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Global Regulatory Lead, Oncology (Associate Director) employer: Consult
At Consult, we pride ourselves on being an exceptional employer that fosters a dynamic and inclusive work culture. Our North America team is dedicated to professional growth, offering robust training and development opportunities while working in a fast-paced, innovative environment. Join us to be part of a collaborative team that values your contributions and supports your career aspirations in the exciting MedTech sector.
