Director, Clinical Quality Assurance

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction. The Director, Clinical Quality Assurance (CQA) will be responsible for the overall operation of Cytokinetics Clinical QA department. They will establish, maintain, and ensure effectiveness of quality programs and documentation to assure compliance in an international regulatory environment. They will lead the CQA group responsible for quality plans, policies, procedures, and quality system elements in support of clinical programs. The Director, CQA will provide guidance on CQA related matters. Responsibilities Develop the GCP QA organizational strategy, manage and develop Clinical QA staff to support and enhance quality improvement initiatives for development programs Develop and implement overall GCP strategy, performance metrics, quality tolerance limits, and analytics reports Proactively streamline and strengthen clinical QA processes across the organization and implement improvements in collaboration with cross-functional teams Lead and ensure inspection readiness activities for internal and external entities Lead and co-host GCP, GLP, GVP inspections Lead and manage a risk-based audit program Manage and support internal audits of GCP and GVP processes, and quality audits of clinical vendors and investigator sites Ensure CQA participation on study teams to provide oversight and guidance Identify compliance gaps and provide remediation recommendations for continuous improvement Review and approve SOPs, audit reports, quality event records as required Create, maintain, and adhere to department operating budget Qualifications Bachelor's degree in life sciences with 12+ years experience in a GCP related discipline Current and strong working knowledge, interpretation/implementation United States Code of Federal Regulations and European regulations and guidance, including ICH-GCP Guidance requirements governing clinical research conduct and pharmacovigilance operations Experience managing and developing staff Able to develop innovative solutions to issues and apply critical thinking to problem solving Able to organize and prioritize projects and CQA activities based on risk Able to effectively communicate vision and expectations to the teams Contract & Work Location Hybrid (as indicated by #LI-HYBRID). Up to 10% travel may be required. Pay Range The expected salary range for this position based on the primary location of South San Francisco, CA is $222,480 - $259,560. Benefits equity in the form of stock options and/or restricted stock units comprehensive health insurance coverage dental insurance coverage vision insurance coverage life insurance coverage disability insurance coverage 401k retirement benefits with employer match learning and wellness stipends paid time off Company Culture & Diversity Our employees come from different backgrounds, and we celebrate those differences. We champion integrity, ethics, doing the right thing, and being our best selves. Cytokinetics is an Equal Opportunity Employer. #J-18808-Ljbffr Cytokinetics