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Program Manager, Clinical Quality Assurance
- Irvine, California, United States
- Irvine, California, United States
Über
Position can be in Irvine, CA or the N. Chicago, IL office (hybrid is an option)...As the primary GCP quality interface cross-functionally in R&D for the product, this individual will influence and provide oversight of activities that include execution of the Comprehensive Quality Strategy game plan, informal surveillance, assessments as appropriate, design and execution of a fit for purpose audit program with the goal of submission-ready quality data, first pass approvals by health authorities for market authorizations, and bringing our compounds to our patients. This is an independent contributor role that will influence across matrix organizations.
Responsibilities:
- Develop and manage project timelines and deliverables for the RDQA Comprehensive Quality Strategy plan, including a lead role in Risk and Issue Management
- Assess the success and effectiveness of the quality system and assure inspection readiness by designing an audit program of internal and external compliance audits and applicable assessments
- Interpret, explain and apply applicable current governmental regulations, guidelines, policies and procedures to study protocols and associated activities
- Prioritize activities to ensure objectives of studies/programs are met
- Interact with Development Operations organization and supporting functions to ensure quality compliance across all aspects of clinical development; Identify and mitigate potential clinical quality risks and escalate to management; Leverage knowledge of clinical development to maintain program oversight and influence proactive quality management through quality related activities; Provide project/program leadership in quality as a team member across clinical development functions
- Anticipate, influence, and determine present and future business needs in support of quality for a drug development program
- Lead the effort to articulate and present an integrated cross-functional and comprehensive quality strategy plan
- Identify and implement balanced fit-for-purpose quality management; Develop and recommend strategies and tactics for success
- Identify and remove barriers that could impact program objectives, priorities, timelines, and quality. Communicate risks and mitigations to management
- Serve as the primary program quality liaison during health authority inspections
Education:
Bachelors degree in a physical science, life science, nursing, pharmacy or equivalent experience required
5+ years of pharmaceutical industry experience in GCP quality assurance or regulatory affairs or clinical development or clinical operations (oncology-specific a plus, but not a requirement). 1+ years of GCP QA auditing and Medical Device experience preferred.
Successful and progressive leadership experience in motivating teams to anticipate and deliver strong operating results, as well as to meet or exceed customer expectations.
Sprachkenntnisse
- English
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