Acadia Pharmaceuticals Inc.

Associate Director TMF Management & Inspection Readiness

Acadia Pharmaceuticals Inc.

2 days ago
Princeton, New Jersey, United States
Hybrid
Full Time
Senior
1 applicant
Acadia Pharmaceuticals Inc.
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About this role

The Associate Director, Trial Master File Oversight & Inspection Readiness at Acadia Pharmaceuticals leads the oversight of clinical documentation and inspection preparedness, ensuring regulatory compliance and audit readiness. This role involves coordinating inspection activities, maintaining documentation standards, and partnering cross-functionally to support clinical trial compliance.

Skills

Acadia Pharmaceuticals Inc.

About Acadia Pharmaceuticals Inc.

acadia.com

Industry

Healthcare

Acadia Pharmaceuticals is a biopharmaceutical company focused on advancing care for underserved neurological disorders and rare diseases. The company works to translate scientific promise into meaningful innovation by progressing novel therapies from research through clinical development and commercialization. Acadia’s portfolio and pipeline prioritize conditions with high unmet medical need, emphasizing patient-centered development and collaboration to accelerate access to new treatments.

About Acadia Pharmaceuticals Inc.

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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