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Clinical Agreements Manager
2 months ago
We are seeking a knowledgeable individual who possesses a deep understanding of the intricacies involved in contract evaluation. The ideal candidate will be adept at analyzing protocols and translating them into comprehensive budgets while adhering to stringent guidelines.
Key Responsibilities:
- Serve as the primary authority for reviewing and processing all Clinical Trial Agreements.
- Conduct thorough evaluations of Confidential Disclosure Agreements (CDAs), Non-Disclosure Agreements (NDAs), and Master Clinical Trial Agreements.
- Collaborate with Clinical Research Faculty and staff to facilitate budget preparation and negotiation.
- Ensure compliance with Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and sponsor policies throughout the Clinical Trial Agreement process.
- Provide training and support for Clinical Trial Management Systems (CTMS) to Clinical Faculty and Staff.
- Monitor and ensure the recovery of all clinical research-related receivables within the CTMS System, working closely with Post Award teams.
- Oversee the management of PACs agreements related to Clinical Trial Agreements and act as the central point of contact for Sponsors and Clinical Research Teams.
- Co-administer the TriNetX and REDCap platforms, along with a comprehensive range of responsibilities within the Clinical Trials Office.
Qualifications:
- Minimum: Bachelor's Degree with a minimum of 3 years of experience in clinical trial research and administration, particularly with clinical trial agreements and management.
- Significant expertise in clinical trial management systems and financial oversight of the clinical trial lifecycle.
- Preferred: Master's Degree in Business, Healthcare, or a related field, along with at least one year of relevant clinical research administration experience. Candidates with a Juris Doctor (JD) degree will also be considered.
Experience Level:
Intermediate Level
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