Clinical Research Assistant

Boston Children’s Hospital; Brookline (MA); Hybrid; USD 60,000 - 75,000; Full time

Job summary

Boston Children’s Hospital is seeking a Clinical Research Coordinator to coordinate daily activities for clinical research studies. You will screen and enroll patients, monitor protocol implementation, collect data, and prepare reports in alignment with study standards.

Responsibilities include obtaining informed consent, coordinating with families, and assisting with regulatory submissions to IRBs. This role supports multiple sites, including on-site and off-site locations, and requires

Qualifications

• Bachelor's degree in a STEM field required.
• 0–1 year of relevant research experience.
• Demonstrated ability to coordinate schedules and communicate clearly.

Responsibilities

• Consents and enrolls patients for research studies.
• Adheres to policies and procedures and responds to inquiries.
• Obtains informed consent and screens patients for inclusion criteria.
• Serves as liaison to families/patients at on-site and off-site locations.
• Coordinates follow-up visits and addresses participant concerns.
• Prepares documentation for IRB submissions and study approvals.

Skills

Communication

Team coordination

Data collection

Regulatory understanding

Education

Bachelor's degree in a STEM field

Job description

Position Summary

Under supervision, coordinates daily activities and operations of clinical research studies. Responsible for screening and enrolling patients, monitoring protocol implementation, completing required forms and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical study standards and procedures to plan and conduct clinical research studies. Maintain open communication with team members to ensure proper study progress.

Key Responsibilities

• Consents and enrolls patients for research studies by providing detailed information on the Research Study to patients and families.
• Is responsible for understanding and adhering to all policies and procedures and responds to all inquiries.
• Obtains informed consent and enrolls patients in research studies. Reviews clinical information to identify patients meeting study inclusion criteria.
• Serves as liaison to the families/patients in the research studies, conducted at both on site and off-site locations, guiding and advising them throughout each phase of the study.
• Coordinates follow up visits as necessary. Acts as a resource to study participants, addressing any concerns they may have.
• Troubleshoots resolution of any issues that may arise throughout the study. Coordinates and prepares documentation needed for Institutional Review Board (IRB) on submissions, for PI approval.
• Tracks progress from submission to approval. Assist in developing supportive study documents such as informed consent forms, monitoring templates, study subject tracking tools, monitoring forms, study manuals, and training materials, as required for a study.
• Assist with the tracking and compilation of enrollment information.
• May assist with preparation of manuscripts and reports to be submitted to academic journals. May help train and orient newly hired study personnel.
• Coordinates activities with various departments to ensure correct testing/processing and sends clear instructions to each study.
• Monitors and reviews data collection and data entry, and informed consent procedures ensuring consistency of application for each study.

Minimum Qualifications

Education:

• A bachelor's degree in a STEM field

Experience:

• 0-1 years of relevant research experience