Role Description
Make an Impact as a Manager, Clinical Trial Management - Oncology at Worldwide. Bring your clinical research and leadership experience to a role where you will help drive the quality and timely delivery of site management services across clinical programs and projects.
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Provide therapeutic and operational expertise throughout the delivery lifecycle.
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Lead and develop assigned clinical research staff.
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Ensure projects have the resources, training, and strategies needed for effective execution.
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Work closely with Project Management, Site Management, Study Start Up, therapeutic teams, and Global Quality Assurance.
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Strengthen collaboration, monitor project health and quality, and develop practical solutions that support successful clinical trial delivery.
What You'll Do
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Lead the quality and timely delivery of site management services provided by assigned Clinical Research Associates across therapeutic programs and projects.
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Provide therapeutic and operational expertise throughout the program and project delivery lifecycle.
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Partner with Project Management, Site Management, Study Start Up, therapeutic teams, and Global Quality Assurance to coordinate clinical delivery and address project needs.
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Develop Clinical Research Associates and Lead Clinical Research Associates through project-specific training.
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Monitor clinical quality and project health through key metrics.
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Serve as a key contact for the Project Management Franchise Lead.
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Identify opportunities to strengthen performance and quality.
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Manage assigned staff, including the quality of their clinical work and appraisal performance reviews.
Qualifications
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A four-year college curriculum with a major concentration in biological, physical, health, pharmacy, or another related science.
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Eight years of clinical research experience as a Clinical Research Associate; or equivalent education/training plus ten years of Clinical Research Associate experience.
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At least two additional years of experience managing Clinical Trial Managers.
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Broad protocol knowledge and a comprehensive understanding of the biopharma industry, drug development lifecycle, and operational clinical trial delivery.
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Strong knowledge of FDA regulations, ICH Guidelines, HIPAA, clinical research principles, and standard operating procedures.
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Experience navigating EDC systems, including platforms such as InForm and Medidata.
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Strong strategic thinking and problem-solving skills.
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Excellent written, verbal, and interpersonal communication skills, including proficiency in English.
Benefits
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Salary range: United States of America - $112,000.00 - $222,000.00 annually.
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Competitive benefits package depending on location.
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Pay equity and transparency.
Company Description
At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.
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More than 4,000 professionals across the globe.
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Collaborative and inclusive environment where diverse perspectives are valued.
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Opportunities to learn, grow, and help shape the future of clinical research.