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Clinical Research Assistant I- Heart Center Clinical Research Program
Boston Children's HospitalUnited Statesfull_timeVerifiedPosted 28 Jul 2025
About the role
Status
Full-Time
Standard Hours per Week
40
Job Posting Category
Research
Job Posting Description
Position Summary/ Department Summary:
Under general supervision, the Clinical Research Assistant working in the Heart Center Clinical Research Program will coordinate daily operations of:
- Several projects involving health outcomes of patients who experienced COVID-related Cardiology symptoms. The CRA working on these studies will be responsible for patient outreach, patient recruitment, data collection, data entry, and overall trial coordination.
- Other ongoing research studies focus on Kawasaki Disease (KD), an inflammatory disease that can cause coronary artery aneurysms. The CRA would be responsible for keeping track of patients who present to BCH with KD in our database and monitoring their follow-up for research studies. The CRA will work closely with multiple MDs and an NP on the KD studies.
- Additional studies include the care and follow-up of patients born with congenital heart disease (CHD), focusing on their care in early stages of life and follow-up for adolescents with CHD.
Key Responsibilities:
- Assists Principal Investigators (PIs) in developing and implementing new clinical research studies and in executing ongoing research studies.
- Coordinates and prepares new protocol applications for submission to the Heart Center’s Scientific Review Committee, the Boston Children's Hospital IRB, and our central IRB at Cincinnati Children’s. Prepares and submits continuing reviews and protocol amendments to the IRB for ongoing studies. Corresponds with the IRB.
- Coordinates weekly meetings with the research teams, including creating the meeting agenda and writing summary documents.
- Recruits study participants for enrollment in clinical research studies.
- Completes data collection through medical record review or through patient visits (study-dependent). Enters clinical data into existing databases in accordance with best practice methods.
- Maintains regulatory binders, case report forms, source documents, and other study documents.
- Complies with all institutional policies and government regulations pertaining to human subjects protection.
Education:
- Bachelor’s Degree required, and a background in university-level science courses would be helpful.
- Prior experience conducting clinical or basic research is preferred, but not required.
Office/Site Location
Boston
Regular, Temporary, Per Diem
Regular
Remote Eligibility
Part Remote/Hybrid
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