Clinical Research Associate

  • Hamilton, NJ
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A bit about us:

We are a publicly-traded global organization, focused on biopharmaceutical solutions.

Why join us?

Strong Compensation
Great Benefits
Equity/Stock Options

Job Details

  • Contribute to all clinical research activities to ensure successful management of clinical studies.
  • Maintain and track clinical study data and support in investigator qualification and selection, analysis of potential patient recruitment, and overall study status/progress throughout the life of a study.
  • Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
  • Serve as main liaison to participating clinical trial sites with focus on data entry, query resolution, investigational device tracking and accountability, and study conduct oversight at the participating clinical sites.
  • Perform on-site and remote site qualification visits, site initiation visits, interim monitoring visits and site close out visits
  • Collaborate with data management to support data cleaning process

  • Bachelor's in biological science, pharmacy or other health related field
  • Ability to perform all clinical monitoring activities independently.
  • Strong and demonstrable planning, management, organization, collaboration and analytical skills
  • An honest and ethical work approach to promote the development of life changing treatments for patients.
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