Description
We are seeking a Clinical Trial Contract Specialist to join our team.
As a Clinical Trial Contract Specialist, you will be responsible for preparing, negotiating, and finalizing clinical trial agreements and ancillary agreements for company-sponsored and investigator-initiated studies.
Key responsibilities include:
- Preparing, negotiating, and finalizing clinical trial agreements and ancillary agreements with clinical trial sites or via oversight of a Clinical Research Organization
- Reviewing and analyzing contractual terms and conditions with global teams
- Assessing legal and budget risks in conjunction with team support functions
- Providing support for negotiations in confidentiality agreements, informed consent forms, and other ancillary contract documents
- Participating in discussions related to the development of site/investigator budgets aligned with fair market value
- Managing the contract amendment lifecycle
- Working with the global CCS team to review and analyze contractual terms to reach resolution
- Proactively providing recommendations to improve processes and establish refinements that reduce cycle time, create savings, and improve efficiency in the initiation of clinical trial sites
- Assuming responsibility for all aspects of legal document and metrics tracking
- Providing support to review, authorize, and understand aspects of site payments
At IQVIA, we create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.