Clinical Research Coord I Endocrine
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About the job
Under moderate supervision of the Principal Investigator, Senior Research Assistant or Manager, the Clinical Research Coordinator I is responsible for a variety of activities in support of clinical research studies.These responsibilities include recruiting and evaluating patients for studies; collecting and organizing patient data; scheduling patients for study visits; maintaining and updating data generated by the study and IRB applications.
Responsibilities
- To provide assistance on clinical research studies as per studies guidelines and protocols.
- Is responsible for the Institutional Review Board submissions and other regulatory forms as well as adhering to the timelines of the study start-up process.
- To assist with the development of the informed consent documents, source documents and other documents as applicable.
- To recruit and evaluate potential study patients.Per protocol instruction, conducts telephone interviews or schedules patients for study visits and screenings.
- To interact with patients/subjects with regards to study, including patient education, procedural instruction, and follow-up.May serve as a liaison between patient and physician.
- Is responsible for collecting data and maintaining patient information database for study.Maybe required to input data, do minimum analysis and run various reports.Maintains patient’s records as part of record keeping function
- To understand and proficiently communicate all components of research documents, such as protocol, informed consent, investigator brochure and research instructions.
- Is responsible for mailing various study information or packets to study participants.
- To answer any phone calls and inquiries regarding study protocol. Refers participants to principal investigator or co-investigators.
- To monitor and set up any needed equipment.
- To interact with study monitors, scheduling monitoring visits as indicated and providing timely responses to study queries.
- To communicate with study participant’s clinical care providers as needed and document research visits within the electronic health record, EPIC, in compliance with institutional policies.
- To maintain inventory and orders supplies when necessary.
- To contribute to a research team environment, serving as back-up coordinator to support other studies in department, cross-training/peer-mentoring other team members and contributing to research meetings.
- All other duties as assigned.
BA or BS degree required.New graduate with relevant course or project work
Primary Location
MA-Boston-BWH Boston Main Campus
Work Locations
BWH Boston Main Campus
Job
Clinical
Organization
Brigham & Women's Hospital(BWH)
Schedule
Full-time
Standard Hours
40
Shift
Day Job
Employee Status
Regular
Recruiting Department
BWH Department Of Medicine / Endocrinology
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