Associate Director, Regulatory Affairs (Onsite in S.SF - 3X/wk)

Role: Associate Director, Regulatory Affairs, based in South San Francisco, supporting clinical regulatory strategies and submissions for biopharmaceutical programs. Objectives: develop and execute global regulatory plans, manage IND applications, and facilitate health authority interactions. Responsibilities: lead regulatory strategy development, prepare INDs and amendments, coordinate with cross-functional teams, provide ongoing guidance on regulations, monitor evolving regulatory landscapes, and drive process improvements. Qualifications: Bachelor's in life sciences with 10+ years' biopharma experience, including 8+ years in regulatory affairs; advanced degrees (MS, PhD, PharmD) preferred. High-value: focus on clinical development, IND management, health authority engagement, with expertise in U.S. and EU regulatory requirements. Skills: strong communication, ability to operate in fast-paced, global environments, integrity, and cross-functional collaboration. Work setup: On-site in South San Francisco, with a competitive compensation package and potential benefits.