This role supports end-to-end research project execution, ensuring timely activation and completion of clinical studies. It coordinates moderately complex projects, manages key documentation, and facilitates cross-functional communication. Responsibilities include negotiating budgets with external sponsors for industry-funded trials, as well as managing internal processes such as CTMS study builds, Medicare Coverage Analysis development and approval, and review of research-related patient charges to ensure compliance and financial accuracy. This position is instrumental in driving efficient, compliant, and financially sound research operations. We are committed to offering flexible work options where approved and stated in the job posting. However, we are currently not considering candidates who reside or plan to reside in the following states: California, Connecticut, Hawaii, Illinois, Massachusetts, Minnesota, New York, Pennsylvania, Rhode Island, Vermont, Washington. Please note that a video interview through Microsoft Teams will be required as well as potential onsite interviews and meetings.
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Job Type
Full-time
Career Level
Mid Level