Tufts University · 7 hours ago
Clinical Research Coordinator
Tufts University School of Medicine is dedicated to improving global health through molecular genetics and innovation. The Clinical Research Coordinator will support day-to-day execution of an observational clinical research study focused on Lyme disease, including participant recruitment, study visits, and specimen logistics.
BiotechnologyHealth CareMedical
Responsibilities
Participant recruitment, screening, consent support
Study visits (in-person, home, remote)
Retention activities & visit reminders
Specimen logistics & shipping (kits, FedEx, courier, lab runs)
Specimen collection coordination & scheduling
Data review
Site support/troubleshooting
General administrative coordination/documentation
Screen and pre-screen potential participants for eligibility using protocol-defined criteria
Coordinate with study physicians and clinical partners to confirm eligibility
Support informed consent discussions and documentation during enrollment visits
Conduct in-person (on-site or home visit) and remote study visits, including administration of study questionnaires and support of sample collection activities
Perform chart abstraction and source document review
Conduct visit reminders and follow-up communications with participants
Support remote data collection sites with sample collection and troubleshooting basic technical issues related to iPads
Ensure all visit activities are completed in accordance with protocol requirement Specimen & Supply Logistics
Prepare, assemble, distribute, and replenish specimen collection kits and study supplies across data collection sites
Travel to the central laboratory to obtain specimen kits and supplies as needed
Transport collected specimens to laboratories in accordance with protocol and biosafety requirements
Maintain inventory of study materials and supplies
Coordinate FedEx shipments, courier pickups, and mobile phlebotomy visits, including scheduling, tracking, and troubleshooting
Ensure proper specimen packaging, labeling, documentation, and shipping supply availability
Communicate shipment or collection issues promptly to the Clinical Research Manager
Assist remote data collection sites with visit preparation and protocol adherence
Provide reminders to remote staff regarding required visit procedures and materials
Troubleshoot basic technical issues with iPads and electronic data collection tools
Communicate issues, deviations, or concerns promptly to the Clinical Research Manager
Maintain participant confidentiality in accordance with HIPAA regulations
Follow institutional policies, study protocols, and standard operating procedures
Escalate protocol compliance concerns to the Clinical Research Manager as needed
Qualification
Required
Knowledge and skills as typically acquired through Bachelor's Degree OR four years of related experience
Preferred
0-2 years experience as a Clinical Research Study Coordinator or equivalent position
Company
Tufts University
With four campuses in Massachusetts, Tufts is a research university committed to helping students and faculty generate bold ideas, innovate, and become active citizens of the world.
Funding
Current Stage
Late StageLeadership Team
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2023-06-30
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