Entry-Level Clinical Research Coordinator – Oncology Trials

massgeneralbrigham; Boston (MA); On-site; USD 65,000 - 85,000; Full time

Job summary

Mass General Brigham is seeking a Clinical Research Associate/Clinical Research Coordinator I to enroll eligible patients into cancer studies and manage data collection. You will liaise with the clinical team, sponsor, and IRB to ensure regulatory compliance and timely reporting.

The role involves data abstraction, regulatory management, and patient coordination, including direct patient contact. You will support screening, scheduling, and sample handling across multiple studies in a fast-paced

Qualifications

• Bachelor's Degree required.
• Clinical Research or compliance experience 1-2 years preferred.
• Regulatory duties may be performed including IRB submissions.

Responsibilities

• Assist clinical team in screening potential patients for study participation.
• Schedule protocol-required tests and procedures and coordinate patient appointments.
• Maintain regulatory binders and prepare protocol amendments and safety reports to IRB.

Skills

Ability to work independently and as a

Analytical skills and ability to solve

Interpret acceptability of data

Education

Bachelor's Degree

Job description

Mass General Brigham is seeking a Clinical Research Associate/Clinical Research Coordinator I to enroll eligible patients into cancer studies and manage data collection. You will liaise with the clinical team, sponsor, and IRB to ensure regulatory compliance and timely reporting.

The role involves data abstraction, regulatory management, and patient coordination, including direct patient contact. You will support screening, scheduling, and sample handling across multiple studies in a fast-paced