Clinical Trials Vendor Associate Director
5 days ago
Job Description:
As a key member of the clinical trial team, you will be responsible for independently managing all clinical vendor-related aspects of global clinical trials. This includes working closely with the study lead and other team members to deliver study outcomes within schedule, budget, quality/compliance and performance standards.
About the Role:
You will serve as the independent leader of the CTT vendor sub-team and a key member of the clinical trial team. Key responsibilities include reviewing and translating vendor-related protocol sections into external service requirements, working with Vendor Start-up Manager on developing the Study Specification Worksheet, and being accountable for vendor cost control, budget review, invoice reconciliation and PO close-out.
- Serve as the independent leader of the CTT vendor sub-team
- Work closely with the study lead and other team members
- Review and translate vendor-related protocol sections into external service requirements
- Develop the Study Specification Worksheet with Vendor Start-up Manager
- Accountable for vendor cost control, budget review, invoice reconciliation and PO close-out
Requirements:
You will require 5+ years of experience in clinical operation processes and direct vendor management, including direct management of key clinical study vendors such as IRT, labs, eCOA, PRR, ECG, imaging. Experience in clinical trial design, mapping to supplier requirements, and the sourcing and contracting of these services is also required. Excellent knowledge of GxP and ICH regulations is necessary.
Benefits:
We offer a collaborative work environment where you can contribute your skills and expertise to help make a meaningful difference in patients' lives. Our company values diversity and inclusion and offers benefits that support a healthy work-life balance.
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