Surgical Oncology Clinical Research Coordinator

Beth Israel Lahey Health; United States; On-site; USD 30,000 - 36,000; Full time

Job summary

Beth Israel Lahey Health is seeking a Clinical Research Coordinator to support the Division of Surgical Oncology in the BIDMC FIRST Program. You will screen and enroll subjects, ensure protocol adherence, and manage data entry and regulatory paperwork.

You will collaborate with clinicians, nurses and research staff to optimize study execution, coordinate scheduling, and assist with insurance approvals and IRB communications, ensuring patient-centered care throughout the research process.

Qualifications

• Bachelor’s degree required.
• 0-1 year of related work experience required.
• Medical terminology.
• Working knowledge of computer systems required, including web-based applications and some Microsoft Office applications.

Responsibilities

• Independently or with other staff, recruits and enrolls research subjects onto clinical research projects per study protocols.
• Checks eligibility criteria against medical records and verifies information with nursing or principal investigator.
• Discusses informed consent with research subjects and assists with scheduling appointments and follow-up tests.
• Learns protocol requirements and ensures adherence to protocols by physicians, nurses and subjects; communicates problems to PI or research nurse.
• Extracts data from hospital records and other sources to complete case report forms; enters data into databases.
• Assists with obtaining insurance approvals and scheduling tests or admissions for subjects.
• Assists investigator with correspondence with IRB.
• As needed, may work in other clinics performing related duties.

Skills

Medical terminology

Written communications

Oral communications

Teamwork

Customer service

Education

Bachelor’s degree

Tools

MS Office

Job description

Beth Israel Lahey Health is seeking a Clinical Research Coordinator to support the Division of Surgical Oncology in the BIDMC FIRST Program. You will screen and enroll subjects, ensure protocol adherence, and manage data entry and regulatory paperwork.

You will collaborate with clinicians, nurses and research staff to optimize study execution, coordinate scheduling, and assist with insurance approvals and IRB communications, ensuring patient-centered care throughout the research process.