ACADIA Pharmaceuticals

Associate Director, Vendor & Relationship Management

ACADIA Pharmaceuticals$145K — $181K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in life sciences or related field, advanced degree preferred.
  • 8 years of experience in clinical trial operations or vendor/CRO oversight in the biopharmaceutical industry.
  • Strong understanding of clinical trial operations and outsourcing models.
  • Experience in managing vendor relationships and performance improvement initiatives.
  • Working knowledge of ICH GCP and regulatory requirements for clinical activities.
  • Strong analytical skills with experience using performance metrics and dashboards.
  • Excellent communication and organizational skills, with ability to influence stakeholders.

Responsibilities

  • Support and execute vendor relationship management strategies, identifying critical partners and managing operational issues.
  • Coordinate vendor governance, facilitating meetings to ensure operational alignment.
  • Develop supplier scorecards and KPIs to monitor vendor performance and trends.
  • Oversee vendor performance for clinical trials, ensuring alignment with timelines and budgets.
  • Collaborate with cross-functional teams to support compliant service delivery and inspection readiness.

Benefits

  • Competitive base salary, bonus, and equity packages.
  • Comprehensive medical, dental, and vision insurance.
  • Employer-paid life, disability, and business travel insurance.
  • 401(k) plan with company match up to 5% fully vested.
  • Employee Stock Purchase Plan with 2-year price lock-in.
  • 15+ vacation days and paid holidays, including a closure between December 24th and January 1st.
  • Paid parental leave and tuition assistance.
Full Job Description
Please note that this position can be based in Princeton, NJ OR San Diego, CA. Acadia's hybrid model requires this role to work in our office three days per week on average.

Position Summary

The Associate Director, Vendor & Relationship Management plays a key role in shaping and strengthening Acadia's strategic partnerships with clinical vendors, CROs, and functional service providers that help advance our innovative clinical development programs. This highly collaborative role will drive vendor governance, performance excellence, and continuous improvement initiatives while fostering a culture of partnership, innovation, and operational excellence across the organization. As a trusted partner to stakeholders across R&D, Procurement, Quality, Finance, and Legal, the Associate Director will help enable effective vendor oversight and consistent outsourcing practices across the Acadia R&D organization.

Primary Responsibilities

Vendor & Relationship Management
  • Support the development and execution of vendor and supplier relationship management strategies, including identification and management of critical partners (CROs, central and specialty labs, functional service providers, clinical technologies, patient recruitment and retention vendors).
  • Serve as a primary point of contact for vendor related operational issues, coordinating resolution and escalating unresolved matters through established governance pathways.
  • Coordinate and facilitate, when appropriate, vendor governance, including operational and steering committee meetings.
  • Develop and maintain supplier scorecards, dashboards, and KPIs to monitor vendor performance and identify trends and risks.
  • Conduct routine business reviews with vendors to ensure alignment on priorities and performance expectations, partnering with Sourcing and Legal as needed.

Operational Oversight & Excellence
  • Oversee vendor performance supporting outsourced clinical trials, through partnership with the Clinica Operations team. Ensure alignment with program timelines, budgets, and quality expectations.
  • Partner with Clinical Operations, Clinical Supply Chain, Quality, Finance, and other cross functional teams to support timely and compliant delivery of services.
  • Support inspection readiness activities, including audits, vendor oversight documentation, and CAPA development in collaboration with Quality.
  • Contribute to process mapping, documentation, and implementation of standardized vendor oversight practices.

Innovation & Continuous Improvement
  • Identify opportunities to improve vendor performance, efficiency, and collaboration through data driven insights and process improvements.
  • Support innovation initiatives within vendor relationships, including new operating models, technologies, or ways of working.
  • Contribute to the development and rollout of best practices, standards, and tools for R&D vendor management.
  • Identify opportunities for cost optimization, demand management, and improved vendor utilization.

Data, Reporting & Technology Enablement
  • Support the development and maintenance of vendor performance reporting and dashboards.
  • Analyze performance metrics to proactively identify risks, issues, and opportunities for improvement.
  • Partner with internal teams to support implementation and optimization of vendor management tools and systems.
  • Act as a mentor and subject matter resource for team members and matrixed stakeholders involved in vendor oversight.
  • Foster strong, collaborative relationships with internal stakeholders and external partners to enable transparent communication and proactive issue resolution.
  • Effectively influence stakeholders across a matrixed organization without direct authority.
  • Other duties as assigned.

Education/Experience/Skills
  • Bachelor's degree in life science or a related field; Advanced degree preferred. Targeting 8 years of experience in clinical trial operations, vendor/CRO oversight, supplier relationship management, or related roles within the biopharmaceutical industry.
  • Experience managing complex vendor relationships and supporting performance improvement initiatives required. An equivalent combination of relevant education and experience may be considered.
  • Strong understanding of clinical trial operations and outsourced service models.
  • Working knowledge of ICH GCP, regulatory requirements, and quality expectations for outsourced clinical activities.
  • Strong analytical skills, including experience with supplier scorecards, KPIs, and performance dashboards.
  • Experience in R&D outsourcing, vendor governance, or business operations functions.
  • Exposure to financial management of outsourced services, including budgeting and accruals.
  • Experience supporting audits, inspections, or inspection readiness activities.
  • Familiarity with alliance or partnership management methodologies.
  • Excellent communication, interpersonal, and organizational skills.
  • Ability to work effectively in a fast paced, matrixed environment while managing multiple priorities and working cross-functionally.
  • 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.

#LI-HYBRID #LI-RE1

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

$145,400-$181,700 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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