Clinical Research Coordinator - Endocrinology

Position: Clinical Research Coordinator I - Endocrinology
Location: St. Louis

* Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants;

resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
* Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
* Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient’s timely completion of protocol requirements; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
* Collects clinical data under clinical research protocols.
* Performs other duties as assigned.
* Registered Dietitian (RD) or equivalent training, or relevant experience in clinical nutrition research
* Experience supporting industry‑ or NIH‑funded clinical studies
* Wet lab skills, including hands‑on laboratory experience
* Experience handling biospecimens, including processing, storage, and sample preparation for shipping
* Ability to work effectively in both patient‑facing and laboratory settings
* Strong organizational skills for sample inventory and study workflow management
* Up to 22 days of vacation, 10 recognized holidays, and sick time.
* Competitive health insurance packages with priority appointments and lower copays/coinsurance.
* Take advantage of our free Metro transit U-Pass for eligible employees.
* WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.
* WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.

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