Clinical Research Coordiantor I at Mass General Brigham
Boston, MA 02115, USA -
Full Time


Start Date

Immediate

Expiry Date

03 Dec, 25

Salary

0.0

Posted On

03 Sep, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Communication Skills, Credentials, Computer Literacy

Industry

Hospital/Health Care

Description

Site: The Brigham and Women’s Hospital, Inc.
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

The CELESTE study seeks a Coordinator to assist with a comparative effectiveness study testing how three therapies for insomnia compare to each other. Following established policies, procedures, and study protocols, the CRC will recruit, randomize, and collect data on study participants across the MGB system, collect adverse event data and ensure timely follow-up by a study physician, and facilitate distribution of study interventions and monitor adherence. The CRC will work closely with study leadership and clinical program staff to operationalize and support study procedures across sites, communicating directly with clinical staff and engaging clinicians. Fluency in English and Spanish are preferred.

QUALIFICATIONS

Education
Bachelor’s Degree Science required
Can this role accept experience in lieu of a degree?
Yes
Licenses and Credentials
Experience
Some relevant research project work 0-1 year preferred

Knowledge, Skills and Abilities

  • Careful attention to detail and good organizational skills.
  • Ability to follow directions.
  • Good interpersonal and communication skills.
  • Computer literacy.
  • Working knowledge of clinical research protocols.
  • Ability to demonstrate respect and professionalism for subjects’ rights and individual needs.

How To Apply:

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Responsibilities

Please refer the Job description for details

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