ACADIA Pharmaceuticals

Senior Director, Clinical Development

ACADIA Pharmaceuticals$306K — $382K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • MD or equivalent required; Board Certified/Eligible strongly preferred.
  • Targeting 5 years of relevant medical/clinical practice, research, or academic experience within the pharmaceutical industry.
  • Experience with medical monitoring and creating development plans for clinical studies is essential.
  • Applicable industry experience across several development phases is strongly desired.
  • Established networks with thought leaders and investigators in mood disorders and rare diseases.

Responsibilities

  • Create and execute global clinical development plans aligned with company goals.
  • Ensure effective execution of clinical studies, including protocol development and data analysis.
  • Build and maintain relationships with investigators and thought leaders in the scientific community.
  • Support patient recruitment and study quality through regular site interactions.
  • Communicate clinical program issues and results to stakeholders promptly.
  • Assist with regulatory interactions, including document submissions and presentations.
  • Provide clinical expertise to facilitate the transition of compounds from discovery to development.

Benefits

  • Competitive base salary and discretionary bonus opportunities.
  • Comprehensive medical, dental, and vision insurance.
  • Employer-paid life, disability, and business travel coverage.
  • Robust 401(k) Plan with a generous company match.
  • Employee Stock Purchase Plan with price lock-in.
  • Generous vacation and paid holiday policy, including office closure during the year-end holidays.
  • Paid sick leave and parental leave benefits available.
  • Tuition assistance to support ongoing education and professional development.
Full Job Description
Position Summary

Join Acadia as the Senior Director, Clinical Development and play a critical leadership role in advancing innovative therapies for neuropsychiatric disorders and rare diseases. In this highly visible position, you will help shape clinical development strategies, provide scientific and medical leadership across development programs, and drive key clinical milestones. Leveraging your deep clinical expertise, strong scientific foundation, and established network within the medical community, you will contribute to the successful design and execution of clinical programs. This is a unique opportunity to impact the development of transformative treatments that improve outcomes for patients with significant unmet medical needs.

Primary Responsibilities
  • Create and execute global clinical development plans consistent with Company 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
  • Other duties as assigned

Education and Experience
  • MD or equivalent required; Board Certified/Eligible strongly preferred. An equivalent combination of relevant education and experience may be considered
  • Targeting 5 years of relevant medical/clinical practice, related research, or academic experience within the pharmaceutical industry
  • Ideal candidate will have experience with medical monitoring, including clinical research, creating and implementing development plans and clinical studies. An equivalent combination of relevant education and experience may be considered
  • Applicable industry experience across several phases of development is strongly desired
  • Established relationships with thought leaders and investigators in depression and other mood disorders
  • Experience in rare disease and/or neurology strongly preferred
  • Demonstrated leadership to work well within a geographically diverse cross-functional team environment
  • Ability to work within a growing organization within and evolve over time into the world leader in psychiatry and neurology, thereby improving the quality of life of those suffering from CNS disorders
  • Experience interacting with senior leaders, including global regulatory agencies
  • Excellent verbal and written communication skills as well as interpersonal, management, and organizational skills
  • Demonstrated problem solving abilities and conflict resolution skills
  • Ability to engage in an open, constructive and continuous dialogue with the Company's stakeholders
  • Highly motivated, self-driven and dependable
  • Willing and able to travel both domestically and internationally

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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In addition to a competitive base salary, this position is also eligible for discretionary bonus and equity awards based on factors such as individual and organizational performance. Actual amounts will vary depending on experience, performance, and location.

Salary Range

$306,100-$382,600 USD

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What we offer US-based Employees:
  • 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

About ACADIA Pharmaceuticals

ACADIA Pharmaceuticals is a biopharmaceutical company focused on the development and commercialization of innovative medicines to address unmet medical needs in central nervous system (CNS) disorders. The company's lead product, Nuplazid (pimavanserin), is the first and only FDA-approved treatment for hallucinations and delusions associated with Parkinson's disease psychosis. ACADIA's pipeline includes product candidates for the treatment of schizophrenia, dementia-related psychosis, and major depressive disorder. The company was founded in 1993 and is headquartered in San Diego, California.
Learn more about ACADIA Pharmaceuticals
Size
500 employees
Market Cap
$2.5 billion
Industry
Net Income
-$281.5 million
Founded
1993
5 Year Trend
+94.6%
Revenue
$441.7 million
NASDAQ

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