ACADIA Pharmaceuticals

Director, External Innovation R&D Program Lead

ACADIA Pharmaceuticals$196K — $245K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant scientific discipline required; advanced degree (PhD, PharmD, MD, or Master's) preferred
  • 10-12 years of industry experience in the pharma or biotech industry
  • Experience in global R&D program management, portfolio strategy or project leadership for clinical-stage programs
  • Strong scientific expertise with the ability to evaluate complex clinical and preclinical data
  • Understanding of drug development, commercialization considerations, and industry dynamics

Responsibilities

  • Lead cross-functional due diligence for external opportunities, coordinating input from multiple stakeholders
  • Develop diligence workplans with key questions, timelines, and risk assessments
  • Build integrated development scenarios and value drivers to inform investment decisions
  • Contribute to integrated opportunity assessments evaluating scientific rationale and clinical development strategy
  • Translate complex data into clear recommendations for senior leadership
  • Support in-licensing and partnership evaluations with Business Development
  • Maintain strong relationships across internal teams to ensure alignment in evaluations

Benefits

  • Competitive base salary and discretionary bonus
  • Medical, dental, and vision insurance
  • 401(k) Plan with company match up to 5%
  • Employee Stock Purchase Plan with purchase price lock-in
  • 15+ vacation days and 13-15 paid holidays
  • Paid parental leave and tuition assistance
Full Job Description
Please note that this position can be based in San Diego, CA, 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 Director, External Innovation will serve as the R&D project lead for external opportunity due diligence, coordinating cross-functional input and leading or co-leading the development of diligence workplans, including key questions, timelines, and risk assessments.

This role will lead cross-functional scientific, clinical, and strategic evaluation of external opportunities aligned with Acadia's corporate strategy and R&D portfolio priorities across neuroscience, psychiatry, neuro-rare, and rare disease areas. The Director will help build preliminary integrated development scenarios, resource assumptions, and value drivers to inform opportunity evaluation, investment decisions, and governance discussions.

Primary Responsibilities:
  • Serve as the R&D project lead for external opportunity due diligence, coordinating cross-functional input from Clinical and Nonclinical Development, Regulatory, CMC, Commercial, Finance, Legal, and other key stakeholders
  • Lead or co-lead the development of diligence workplans, including key questions, timelines, risk assessments, decision frameworks, and preliminary integrated development scenarios, resource assumptions, and value drivers to inform investment decisions
  • Build preliminary integrated development scenarios, resource assumptions, and value drivers to inform diligence and investment decisions
  • Contribute to the development of integrated opportunity assessments that evaluate scientific rationale, clinical development strategy, unmet need, competitive differentiation, regulatory considerations, development risk, commercial potential, and strategic fit
  • Translate complex scientific, clinical, competitive, and financial information into clear recommendations for senior leadership and governance decision-making
  • Partner with Business Development to support in-licensing, acquisition, collaboration, and partnership evaluations, including preparation of internal business cases and transaction-related materials
  • Provide strategic input into therapeutic area and portfolio prioritization based on external landscape trends, emerging science, competitive activity, and internal capabilities
  • Build and maintain strong relationships with internal R&D, Commercial, Finance, Legal, and business stakeholders to ensure alignment throughout evaluation and diligence processes
  • Represent Acadia in external scientific, biotech, academic, and industry interactions as appropriate to support opportunity evaluation and external innovation efforts
  • Contribute to knowledge management, diligence best practices, evaluation templates, and consistent decision frameworks across external opportunities
  • Perform other duties as assigned

Education/Experience/Skills:
  • Bachelor's degree in a relevant scientific discipline required; advanced degree (PhD, PharmD, MD, or Master's) preferred
  • 10-12 years of industry experience in the pharma or biotech industry
  • Experience in global R&D program management, portfolio strategy or project leadership for clinical-stage programs is required
  • Experience leading cross-functional asset evaluations, scientific due diligence, portfolio assessments, and/or drug development strategy initiatives
  • Strong scientific expertise with the ability to evaluate complex clinical and preclinical data
  • Experience in neuroscience and/or rare disease (neurologic/psychiatric and/or non-neuro rare disease) preferred
  • Understanding of drug development, commercialization considerations, and industry dynamics
  • Ability to synthesize complex information into clear, actionable insights for senior stakeholders
  • Strong cross-functional collaboration and influencing skills in a matrixed environment
  • Working knowledge of transaction processes, due diligence, and partnership structures
  • Experience developing strategic recommendations and governance materials for senior leadership and investment decision-making
  • Experience integrating scientific, clinical, regulatory, commercial, and financial considerations into asset evaluations and portfolio recommendations
  • Experience supporting or leading external opportunity assessments, due diligence activities, and cross-functional evaluation teams
  • Ability to manage multiple priorities and operate effectively in a fast-paced environment
  • Ability to travel domestically and internationally as required

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 both in a standard office environment and while working independently from remote locations. 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 schedule or business needs.

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

$196,000-$245,200 USD

#LI-HYBRID #LI-MS1

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

$236,200-$295,300 USD

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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