Oncology Clinical Research Coordinator I

Mass General Brigham; Boston (MA); On-site; USD 28,000 - 40,000; Full time

Job summary

Mass General Brigham's General Hospital Corporation seeks a Clinical Research Associate/Coordinator I to support cancer protocols, enroll patients, and manage data collection and reporting. You will liaise with the clinical team, sponsor, and IRB to ensure compliant communication and accurate data entry.

The role covers screening, scheduling, coordinating visits, tissue processing, and safety monitoring. A bachelor’s degree and 1–2 years of clinical research experience are preferred; onsite at

Qualifications

• Bachelor’s Degree in a related field required.
• Clinical Research or compliance experience 1–2 years preferred.
• Ability to work independently and as a team member.
• Analytical skills and problem-solving ability.
• Attention to detail and strong organizational skills.
• Good communication and understanding of protocol requirements.

Responsibilities

• Screen potential patients for study participation and enroll as required.
• Schedule protocol tests, procedures, and doctor visits.
• Coordinate appointments with physicians, nurses, and test areas.
• Coordinate safety lab specimen collection and timely results.
• Prepare pre-visit communications for providers.
• Maintain front-line communication with enrolled patients.
• Develop protocol-specific flow charts and intake tools.
• Arrange tissue sample processing and correlate lab work.
• Obtain vital signs and perform EKGs as required.
• Administer quality of life assessments per protocol.
• Verify consent and eligibility criteria; monitor enrollment.
• Monitor adverse events and deviations; report to sponsors.
• Maintain study regulatory binders and source documents.
• Prepare regulatory submissions and amendments to IRB.

Skills

Attention to detail

Organizational skills

Follow directions

Communication skills

Computer literacy

Clinical research protocols

Professionalism

Education

Bachelor’s degree in related field

Job description

Mass General Brigham's General Hospital Corporation seeks a Clinical Research Associate/Coordinator I to support cancer protocols, enroll patients, and manage data collection and reporting. You will liaise with the clinical team, sponsor, and IRB to ensure compliant communication and accurate data entry.

The role covers screening, scheduling, coordinating visits, tissue processing, and safety monitoring. A bachelor’s degree and 1–2 years of clinical research experience are preferred; onsite at