Sr. Program Manager, Drug Development

Role: Lead cross-functional drug development programs from pre-clinical through regulatory approval at Neurocrine Biosciences, focusing on neurological, psychiatric, endocrine, and immunological disorders. Responsibilities: develop and execute integrated program strategies, manage schedules, assess and mitigate risks, facilitate stakeholder communication, and support process improvements. Direct or advise on project planning, resource allocation, and milestone tracking, ensuring alignment across research, CMC, clinical, regulatory, and commercial teams. Qualifications: BS/BA in Life Sciences with 8+ years or Master’s in Life Sciences with 6+ years, or PhD with 4+ years in pharma/biotech; experience managing global drug development efforts including IND/CTA, NDA/MAA submissions; PMP certification preferred. Skills include leadership, cross-functional collaboration, project management software proficiency, and in-depth knowledge of drug development processes across phases. HighValue: experience with early and late-phase global programs, regulatory submissions, and complex project coordination. WorkSetup: not specified.