Senior Director, Clinical Development

Acadia Pharmaceuticals Inc.•San Diego, CA

7d•$306,100 - $382,600•Hybrid

About The Position

Join Acadia as a Senior Director, Clinical Development and play a key leadership role in advancing innovative therapies for neurodegenerative and psychiatric disorders. In this position, you will provide scientific and medical leadership across clinical development programs, guiding strategy, study execution, and regulatory interactions. You will partner with investigators, key opinion leaders, and cross-functional teams to drive the successful development of innovative CNS therapies. This is an exciting opportunity to influence programs from development through lifecycle management while helping address significant unmet patient needs.

Requirements

MD, MD-PhD, or equivalent medical degree required; Board Certified or Board Eligible in Psychiatry or Neurology
Minimum 5+ years’ applicable industry across several phases of development is desired
CNS clinical research experience is required, including demonstrable experience in successfully creating and implementing development plans and clinical studies; demonstrable experience in neurodegenerative and / or psychiatric disorders is preferred
Established relationships with thought leaders and investigators in neurodegenerative and / or psychiatric disorders and other mood disorders
Demonstrated ability to work well within a geographically diverse team structure
Ability to work within a growing organization within the U.S. and to help the organization evolve over time into the world leader in psychiatry and neurology, thereby improving the quality of life of those suffering from central nervous system disorders
Ability to engage in an open, constructive and continuous dialogue with the Company’s stakeholders based on equality and mutual respect; transparency is critical and a key element to success
Effective oral and written communication skills
Highly motivated, self-driven and dependable
Ability to travel domestically and internationally as business needs require

Responsibilities

Create and execute global clinical development plans consistent with the Company’s strategic vision and mission
Ensure the optimal planning, implementation and interpretation of clinical studies, including synopsis/protocol development, medical monitoring, data analysis and writing of final reports
Maintain and build productive relationships with investigators, thought leaders and centers of excellence across the scientific community, as well as with colleagues across the Acadia organization
Interact frequently with sites to support study awareness, patient recruitment, and quality of study conduct
Communicate appropriate program issues and results to key internal and external stakeholders
Support regulatory interactions, including the submission of regulatory documents and presentations
Provide clear and insightful clinical and scientific expertise to advance the successful transition of compounds from discovery to full development, and subsequently to life cycle management
Review business development opportunities, translating business needs to cost-effective development strategies that provide a competitive advantage and meet regulatory requirements
Comply with current local and international regulations, laws, scientific and regulatory guidance, Good Clinical Practices, and Acadia’s policies and procedures

Benefits

Competitive base, bonus, new hire and ongoing equity packages
Medical, dental, and vision insurance
Employer-paid life, disability, business travel and EAP coverage
401(k) Plan with a fully vested company match 1:1 up to 5%
Employee Stock Purchase Plan with a 2-year purchase price lock-in
15+ vacation days
13 -15 paid holidays, including office closure between December 24th and January 1st
10 days of paid sick time
Paid parental leave benefit
Tuition assistance