[Hiring] Clinical Program Quality Manager @USA - 3316 Takeda Development Center Americas, Inc.

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role DescriptionTakeda Development Center Americas, Inc. is seeking a Clinical Program Quality Manager with the following duties:• Support GCP compliance activities for oncology clinical trials through the development and implementation of program-specific, risk-based audit and compliance strategies• Conduct audits of investigator sites, clinical documentation, vendors, and internal systems to ensure adherence to GCP, regulatory requirements, and internal policies• Assess audit findings and compliance risks, with a focus on subject safety, data integrity, and operational impact, and escalate significant issues to management• Manage Takeda and CRO-related quality investigations, ensuring they are comprehensive, timely, and compliant with SOPs and regulatory expectations• Perform Principal Investigator (PI) checks prior to study initiation by reviewing audit and quality investigation reports to confirm investigator readiness and compliance history• Provide support during regulatory inspections, including preparation of responses and coordination of follow-up actions• Collaborate with cross-functional teams and quality functions to identify and mitigate systemic GCP compliance issues across oncology programs• Analyze and report compliance metrics to development teams and leadership, ensuring accurate documentation and timely communication• Leverage prior experience in managing QMS documentation, governance materials, and operational oversight to support continuous improvement of quality systems and processes• Contribute to the development of tools, templates, and guidance to enhance inspection readiness and quality oversight across clinical programs• Analyze, report, and present metrics for assigned programs to development teams and CPMQ management• Recommend any required actions and monitor implementation100% remote work allowed from anywhere in the U.S.Qualifications• Bachelor’s degree in Pharmacy, Regulatory Affairs, Clinical or related field• 5 years of related experience• Implement knowledge of the applicable GCP and GVP regulations and guidance and ICH Guidelines to support the study team• Identify and investigate the quality issues related to the functional processes• Analyze and assess the risk and impact of the quality events and develop appropriate corrective and preventive actions to improve the processes• Manage and track team projects, their timelines, and deliverables to ensure their completion in a timely mannerRequirements• Full time• $116,000.00-$196,000.00 per yearCompany DescriptionTakeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do.We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own. Takeda is an equal opportunity employer. Apply tot his job