Number of Applicants
:000+
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Please note that this position can be based in San Diego, CA OR San Francisco, CA OR Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average.
Position Summary
The Executive Director will lead the design and implementation of disease and drug mechanism of action (MoA) studies to advance therapeutics into and through clinical development. The position requires deep experience in translational sciences, proven leadership and mentoring skills, hands-on rare disease experience, strong understanding of clinical biomarker development, and a deep understanding of drug development from discovery through late-stage clinical studies. The ability to synthesize complex biological concepts and data into clearly communicated actionable insights is critical, as is a track record of successful partnering with functions across the drug development paradigm.
Primary Responsibilities
Develop translational biology strategies to interrogate disease and drug MoA, implement and drive execution for candidate targets and therapeutics
Lead nonclinical sciences function, mentor scientists across translational sciences
Partners with colleagues across the drug development paradigm to develop and test hypotheses designed to advance target and candidate molecule evaluation through various stages of development
Partner with Translational Science colleagues to develop preclinical strategies supporting indication selection, PK/PD analyses, and mechanistic development for successful IND filing and clinical development
Synthesize, analyze and integrate complex biological data, providing clear and actionable insights to drive drug development decisions
Identify, evaluate and leverage cutting-edge technologies to expedite early-stage program development & success
Identify and manage CROs and build strong collaborative relationships with Acadia partners to maximize the application of complementary areas of expertise
Present programs and data for asset team, governance and senior / executive management review
Contribute, as author and strategist, to document generation for preclinical studies & clinical protocols, clinical study reports, statistical analysis plans, research partnerships, regulatory materials (IB, IND, NDA, etc.) and publications
Perform other responsibilities as assigned
Education/Experience/Skills
PhD in life science or related field. Targeting 15 years of progressively responsible experience in drug development within the pharmaceutical or biotech industry. An equivalent combination of relevant education and experience may be considered.
Key Skills:
Physical Requirements
This role involves regular standing, walking, sitting, and the use of hands for handling or operating equipment. The employee may also need to reach, climb, balance, stoop, kneel, crouch, and maintain visual, verbal, and auditory communication in a standard office environment and while working independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. This position requires the ability to travel independently overnight and/or work after hours as required by travel schedules or business needs.
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