Clinical Research Coordinator
1 day ago
Job Summary:
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at Mass General Brigham. The successful candidate will be responsible for supporting all aspects of clinical research coordination for studies at our institution.
Key Responsibilities:
- Coordinate all activities of subjects participating in individual research studies, including scheduling patients and collecting and documenting patient data.
- Maintain accurate records and databases.
- Assist with recruiting patients for clinical trials.
- Obtain patient study data from medical records and verify the accuracy of study forms.
- Prepare data for analysis and data entry.
- Assist with regulatory binders and QA/QC procedures.
- Administer and score questionnaires.
- Provide basic explanations of study procedures and obtain informed consent from subjects.
- Perform study procedures such as phlebotomy, vital signs, and electrocardiogram.
- Correspond with the Institutional Review Board (IRB) for approval of protocol, notification of adverse events, and submission of amendments.
Requirements:
- Bachelor's degree required.
- Relevant coursework or project experience.
- Understanding of federal regulations, IRB review process, informed consent, trial design, and data monitoring.
- Good writing and editing skills.
- Prior experience working in clinical research is a plus.
Working Conditions:
Office work with occasional travel. May be exposed to dry ice and -80-degree freezers. May have to lift up to 20lbs and apply force to resist patients/subjects in hand-held dynamometry. May be exposed to bodily fluids, including blood, urine, and cerebral spinal fluid. May work at different MGH or MGB sites.
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