Research Technician II

Mass General Brigham•Boston, MA

7d•Onsite

About The Position

Enrolls eligible patients to clinical research protocols and manages data collection and regulatory submissions for multiple cancer studies. Serves as the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting. The position involves a high volume of data abstraction and data entry.

Requirements

Bachelor's Degree Related Field of Study required
1-2 years related research experience required
Ability to work independently and as a team member.
Good organization and communication skills.
High degree of computer literacy.
Proficient analytical skills and ability to resolve problems.
Ability to interpret acceptability of data results.
Careful attention to detail.
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Responsibilities

Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all criteria
Enroll patients as required by the study sponsor and internal enrollment monitor team
Follow patients for the duration of study participation via electronic medical record review to ensure protocol compliance
Monitor and report adverse events and deviations as required by the sponsor, institution, and federal regulations
Maintain research charts and/or electronic files for all enrolled patients
Communicate protocol clarifications from the study sponsor
Schedule and prepare for monitoring visits and audits
Collect, complete, and submit essential regulatory documents and protocol information to various regulatory entities (IRB)