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Clinical Research Coordinator

Insight Global
Rockville, MD
  • Expired: over a month ago. Applications are no longer accepted.
Job Description


Our large government client is seeking a biomedical scientist with experience managing medical information and clinical products associated with longitudinal studies. This research study collects a wide variety of data from sources including biospecimens, physical measurements, genomic profiles, mobile health devices, and medical histories to describe a cohort of over a million people who will be followed for over 10 years.

In support of the program, we are seeking a dedicated individual who can assist in the development, management, and overall stewardship of program governance, collaborations, protocol development, and program policies. Additional Responsibilities Include:

  • Building and managing collaborations between internal divisions and awardees
  • Developing, managing, or supporting a number of internal processes relating to clinical study
  • Understanding the wealth of available healthcare data to assist the program in data sourcing, interpretation, and utilization.



  • Master's degree in Biomedical sciences or Public Health
  • Minimum of 2 years of industry experience in longitudinal research studies
  • Experience working in the project management aspects of clinical trials and research studies such as:
    • Programming or administration of Jira and other Atlassian products
    • Pediatric studies or clinical trials
    • Running clinical or survey pilots, protocol writing, and IRB (institutional review board) submission experience.
    • Managing Communications or Collaborations of large groups


  • Experience working with government agencies for research studies or clinical trials

Insight Global

Why Work Here?
Sign on bonus, annual merit increases: 8% bonus, $45 mobile allowance, relocation packages starting at $2,5000-10,000


Rockville, MD




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