Clinical Research Coordinator I

Beth Israel Lahey Health•Burlington, VT

1d•Onsite

About The Position

Under general supervision and direction, the Clinical Research Coordinator I will be responsible for the coordination and administration of multiple research studies. This role involves working closely with principal investigators and research staff to facilitate all aspects of assigned clinical trials, ensuring implementation of study protocols in accordance with regulatory and institutional requirements. The coordinator will set up administrative systems to manage study progress, screen, recruit, and follow study participants, and collect and report study data. The position requires interaction with study participants diagnosed with various medical conditions and diagnoses.

Requirements

Bachelor’s degree required.
0-2 years of experience in a research or medical setting.
Ability to address problems that are routine, somewhat repetitive and generally solved by following clear directions and procedures.
Ability to travel nationally to other research sites, attend investigator meetings and educational conferences as required.
Strong organizational, multi-tasking, attention to detail and communication skills.
Ability to take direction, set priorities and work somewhat independently.
Ability to demonstrate a positive attitude and respond to request in a timely and respectful manner.
Ability to work in small teams, interact with professional personnel at all levels of an organization, and work with study participants of various diseases compassionately and respectfully.
Experience with computer systems, including web-based applications.
Ability to be thoroughly trained to meet organizational standards (in the absence of any of these skills).

Responsibilities

Coordinate and administer multiple research studies.
Work closely with principal investigators and research staff facilitating all aspects of assigned clinical trials.
Implement study protocols in accordance to regulatory and institutional requirements.
Set up administrative systems to manage the progress of each study.
Screen, recruit and follow study participants.
Collect and report study data.
Interact with study participants diagnosed with various medical conditions and diagnoses.
Travel nationally to other research sites, attend investigator meetings and educational conferences as required.