×
Register Here to Apply for Jobs or Post Jobs. X

Clinical Research Coordinator – Massachusetts General Hospital and Harvard Medical School

Job in Harvard, Worcester County, Massachusetts, 01451, USA
Listing for: International Society for Contemplative Research
Full Time position
Listed on 2026-02-07
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
  • Research/Development
    Clinical Research, Medical Science
Job Description & How to Apply Below
Position: Clinical Research Coordinator I – Massachusetts General Hospital and Harvard Medical School
Location: Harvard

Clinical Research Coordinator I – Massachusetts General Hospital and Harvard Medical School

A position is available within the Meditation Research Program (Principal Investigator [PI]: Matthew

D. Sacchet, Ph.D.; website: (Use the "Apply for this Job" box below).) at Massachusetts General Hospital and Harvard Medical School. Our research is in affiliation with the Department of Psychiatry and the Martinos Center for Biomedical Imaging and is focused on developing a scientific understanding of advanced meditation (skills, states, stages, and transformations related to mastery and continued practice of meditation). Ongoing appointment is contingent upon performance and continued availability of funding This position offers an excellent opportunity for junior scientists looking for research experience before applying to graduate school in the mind sciences (including neuroscience and clinical psychology Ph.D. programs) or medical school, or related positions in industry.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

  • Collects and organizes data from research participants
  • Maintains records and databases
  • Uses various software and programs for data analysis, graph generation, and reports
  • Assists with recruiting research participants
  • Obtains participant study data from medical records, physicians, et cetera
  • Conducts literature searches
  • Verifies accuracy of study forms
  • Updates study forms per protocol
  • Documents study participant visits and procedures
  • Assists with regulatory binders and quality assurance/quality control (QA/QC) procedures
  • Assists with interviewing study participants
  • Provides explanation of study and obtains informed consent from study participants
  • Performs study procedures.
  • Assists with study regulatory submissions
  • Writes consent forms

SKILLS/ABILITIES/COMPETENCIES

REQUIRED:

  • High attention to detail
  • Excellent organizational skills
  • Excellent ability to follow directions
  • Working knowledge of research
  • Ability to demonstrate respect and professionalism for other team members and research subjects

EDUCATION:

EXPERIENCE:

New graduates may be considered for the position outlined above. Value will be placed on proven experience with research and commitment to science.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary