Clinical Research Coordinator II

Mass General Brigham•Boston, MA

2d•$24 - $35•Onsite

About The Position

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary coverletter required to be considered for this position Working under general supervision from the Principal Investigator, Senior Project Manager, and following established policies and procedures, the CRC II will provide direct assistance on clinical research study start-up, study implementation as well as coordinate all clinical research and administrative procedures per the study protocol for the successful management of clinical trials.

Requirements

Bachelor's Degree Science required
Can this role accept experience in lieu of a degree? Yes
Related post-bachelor's degree research experience 1-2 years required
Ability to work more independently and as a team member.
Computer literacy, analytical skills, and ability to resolve technical problems.
Ability to interpret the acceptability of data results.
Working knowledge of data management programs.

Responsibilities

Provide assistance on clinical research studies as per studies guidelines and protocols.
Oversee and/or responsible for the Institutional Review Board (IRB) submissions and other regulatory forms and adhering to the timelines of the study start-up process.
Develop informed consent documents, source documents, and other documents as applicable.
Recruit and evaluate potential study participants.
Adhere to protocol requirements for all study conduct.
May be required to perform clinical tests such as phlebotomy, EKG’s, vital signs, coordinate visits and specimen collection.
Interact with potential study participants and study participants to implement protocol with fidelity.
Provide participant education, procedural instruction, and follow-up.
Serve as a liaison between study participant and research team.
Responsible for collecting data and maintaining participant information database for study.
May be required to input data, do minimum analysis and run various reports.
Support the safety of clinical research participants.
Understand and proficiently communicate all components of research documents, such as protocol, informed consent, investigator brochure and research instructions.
Responsible for using all types of communication methods for various studies to study participants.
Answer any phone calls and inquiries regarding study protocol.
Refer participants to principal investigator or co-investigators as clinically indicated.
Responsible for training and orienting new staff.
May serve as a team leader or in a supervisory capacity in a smaller area.
Interact with study monitors, scheduling monitoring visits as indicated, and providing timely responses to study queries.
Maintain study inventory and order study supplies when necessary.
Ensures the appropriate delegation of study related tasks (i.e.: Delegation of Authority) on all protocols.
Communicate with participant’s clinical care providers as needed and document research visits within electronic health record system, in compliance with institutional policies.
Contribute to research team environment, serving as back-up coordinator to support other studies in department, cross-training/peer-mentoring other team members, and contributing to research meetings.
All other duties as assigned.