$80K - $100K*
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.
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
Valid through: 2020-5-19
$200K - $250K
4 days ago