Clinical Research Coordinator I

Mass General Brigham•Boston, MA

4d•$21 - $29•Onsite

About The Position

Following established policies, procedures, and study protocols, the Clinical Research Coordinator I provides assistance on clinical research studies. Work includes recruiting, evaluating, and consenting patients; collecting and organizing patient data; scheduling study visits; performing clinical tests such as phlebotomy and EKGs; and maintaining and updating study data. Candidates completing a bachelor's degree may provide degree-equivalency verification within six months of hire, or within one year if starting per diem.

Requirements

Bachelor's degree in a related field required; experience may be accepted in lieu of a degree.
Careful attention to detail and good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
Computer literacy.
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Nice To Haves

Some relevant research project work; 0–1 year preferred.

Responsibilities

Review proposals for compliance with sponsor and organizational guidelines and verify that sponsor requirements are met.
Recruit patients for clinical trials and conduct phone interviews.
Verify the accuracy of study forms and update them according to protocol.
Prepare data for analysis and data entry.
Document patient visits and procedures.
Assist with regulatory binders and QA/QC procedures.
Assist with interviewing study subjects.
Assist with study regulatory submissions.
Collect and organize patient data, schedule study visits, perform clinical tests, and maintain and update study data.