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Director, Global Regulatory Strategy & Submissions

Cedent Consulting, Cambridge

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An established industry player is seeking a seasoned Regulatory Affairs professional to lead regulatory strategies from early development to late-stage clinical programs. This role involves direct interaction with the FDA and global regulatory agencies, where you'll prepare and lead submissions while ensuring compliance with all regulatory requirements. With over a decade of experience in the pharmaceutical or biotechnology sectors, you'll leverage your expertise to guide internal teams and identify regulatory opportunities. Join a dynamic environment where your contributions will directly impact the success of innovative therapies in the market.
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