Senior Director Regulatory Affairs
clark davis associatesWhite Plains, NY
Senior Director Regulatory Affairs
clark davis associatesWhite Plains, NYManager L7
Pharmaceutical Preparation ManufacturingResearch and Development in BiotechnologyBiological Product Manufacturing
APPLY NOW (opens in a new tab)Senior Director, Regulatory Affairs - Hybrid NYC AreaKey Responsibilities Develop and execute regulatory strategies supporting clinical development and future product approvals. Lead and support preparation and submission of regulatory filings, including INDs, NDAs, and international submissions. Provide regulatory guidance to cross-functional teams throughout the product development lifecycle. Ensure compliance with FDA and global regulatory requirements while monitoring evolving regulations and industry guidance. Identify regulatory risks and develop mitigation strategies. Support regulatory aspects of quality systems, including GCP and GLP compliance.
Qualifications:
Advanced degree with 10+ years of regulatory affairs experience, or Bachelor's degree with 12+ years of relevant experience.
Strong knowledge of FDA and global regulatory frameworks (including Europe and Asia-Pacific markets).Proven experience developing regulatory strategy and managing clinical regulatory submissions.
Excellent communication, collaboration, and project management skills.
Ability to operate as a senior individual contributor in a fast-paced biotech or pharmaceutical environment.
Oncology regulatory experience is required.
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Level
Manager L7
Location
White Plains, NY
Occupation
Regulatory Affairs Managers
Industry
Pharmaceutical Preparation Manufacturing
Posted
22 days ago