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Sr. Manager/Manager R&D Quality Assurance in San Diego, CA



$80K - $100K*


Quality Management, Life Sciences


5 - 7 years

Job Description

Position Summary:

Responsible for implementing, supporting and maintaining the good R&D practice standards to infuse quality, promote compliance mindedness, improve efficiency, and enhance risk management within ACADIA Pharmaceuticals. Informs and executes process improvements and plays a key role with the entire Inspection Readiness Program to identify, address, and mitigate compliance risk areas related to any Company late-phase asset. Serves as the compliance expert, and provides leadership, in GCP and GLP compliance.

Primary Responsibilities:

Responsible for assisting in the management the Master Audit Plan for R&D Quality Assurance to schedule all assigned audits, eg, CSP, Investigator Sites, Documents, and eTMF. Functions as R&D QA study Lead to ensure study specific investigator site audits are included within the MAP. Participates

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Valid through: 2020-5-19

About ACADIA Pharmaceuticals

ACADIA Pharmaceuticals, Inc. is a biopharmaceutical company. The company has a portfolio of four product candidates, including pimavanserin, which is in Phase IV development as a treatment for Parkinsons disease psychosis. It is also developing AGN XX/YY, a product candidate in Phase II for chronic pain; and AC-262271, a product candidate in Phase I for glaucoma, both in collaboration with Allergan, as well as AM-831, a product candidate in IND-track development for schizophrenia in collaboration with Meiji Seika Kaisha. The product candidates in the company'?s pipeline emanate from discoveries made using its proprietary drug discovery platform. Acadia Pharmaceuticals extended its drug discovery and development research agreement with Allergan to March 2012.[citation needed] The agreement stipulates both parties will work together for the discovery of new therapeutics for glaucoma and ophthalmic conditions.
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