Clinical Research Coordinator I, Center for Clinical Investigation

Mass General Brigham•Boston, MA

1d•$21 - $29•Hybrid

About The Position

The Clinical Research Coordinator I works under general supervision from a manager, lead coordinator, or Principal Investigator to support clinical research studies at the Center for Clinical Investigation. The role coordinates sponsored studies, recruits and screens participants, assists with assessing participant suitability, and may perform clinical procedures such as phlebotomy and ECGs. The coordinator also supports participant education and follow-up, study data collection and quality control, regulatory documentation, and administrative activities. The position may involve work across multiple hospital locations and handling biological specimens and electronic equipment.

Requirements

Bachelor of Science or Bachelor of Arts degree; equivalent experience or research certification is acceptable.
Ability to work independently.
Excellent interpersonal skills for working with study participants.
Good oral and written communication skills.
Analytical skills and ability to resolve technical or research problems and interpret the acceptability of data results.
High degree of computer literacy.
Excellent organizational skills and ability to prioritize a variety of tasks.
Careful attention to detail.
Ability to demonstrate professionalism and respect for participants’ rights and individual needs.
Knowledge of data management programs.

Nice To Haves

Some knowledge of medical terminology, clinical practice, and/or research studies is highly desired.

Responsibilities

Coordinate the internal and external implementation of sponsored clinical research studies.
Initiate and maintain recruitment contact with study participants; screen applicants against study criteria and exercise independent judgment about suitability for participation.
Develop and implement participant recruitment strategies in collaboration with the Principal Investigator, Research Manager, and experienced coordinators.
Perform applicable clinical tests, which may include phlebotomy and ECGs.
Work with the RCNet Manager and CCI Administrative Director on administrative duties related to CCI/RCNet programs.
Educate participants, provide procedural instructions and follow-up, and serve as a liaison between participants and physicians and as a resource for participants and their families.
Collect study data and maintain participant information databases; develop, organize, and maintain study forms.
Conduct data validation and quality control, enter data into case report forms when applicable, and potentially perform basic analysis and generate reports.
Complete institutional review board regulatory paperwork in conjunction with the Research Manager.
Mail study information and packets to participants.
Answer calls and inquiries about study protocols and refer participants to principal or co-investigators when appropriate.
Communicate regularly with Principal Investigators about all aspects of the research trial.