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Clinical Research Coordinator I

Mass General BrighamBoston, MA
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. Under general supervision of the Director, the Clinical Research Coordinator provides support for national, multi-year studies and projects at the Research on Emergency Systems, Population Needs and Delivery (RESPOND) Lab (https://mesk.mgh.harvard.edu/). The Clinical Research Coordinator will work principally on a multicenter, multi-year randomized controlled trial of an intervention to reduce unmet oral health and social needs in the ED. The study will assess individual, health system and community level impacts of an intervention to identify and address adverse social determinants of health (aSDoH) along with unmet oral health needs among ED patients. The coordinator may also work on other studies, as needed. Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.

Requirements

  • Bachelor's Degree Science required (or experience in lieu of a degree)
  • Some relevant research project work
  • 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

Nice To Haves

  • 0-1 year preferred experience

Responsibilities

  • Review proposals for compliance with sponsor and organizational guidelines; verify that all sponsor requirements are met.
  • Recruit patients for clinical trials and conduct phone interviews.
  • Verify the accuracy of study forms and update them per protocol.
  • Prepare data for analysis and data entry.
  • Document patient visits and procedures.
  • Assist with regulatory binders and QA/QC Procedures.
  • Assist with interviewing study subjects.
  • Assist with study regulator submissions.
  • Evaluate and consent patients for studies.
  • Collect and organize patient data.
  • Schedule patients for study visits.
  • Perform clinical tests such as phlebotomy, EKGs, etc.
  • Maintain and update data generated by the study.

Benefits

  • Comprehensive benefits
  • Career advancement opportunities
  • Differentials
  • Premiums
  • Bonuses
  • Recognition programs

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Number of Employees

5,001-10,000 employees

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