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Clinical Research Coordinator (RN/LPN)


The RN/LPN Clinical Research Coordinator will be responsible for performing the day-to-day research and administrative activities of clinical trials, including the implementation, data management, and follow-up to assure data accuracy, patient safety, protocol compliance, and regulatory compliance as required by the clinical trial protocol, the study sponsor, and ICH/GCP standards. This individual will coordinate Phase II-IV trials from initial Sponsor contact for site selection, study preparation and initiation to study completion and close-out.

Requirements for this position include experience including but not limited to:

  • Patient Recruitment/Screening/ICF process
  • IRB Submissions
  • Patient Scheduling
  • Following GCP’s
  • Prepare Source Documentation and Complete CRF forms in timely manner
  • Communicate study needs to principal investigator and other research coordinators
  • Sponsor Relations
  • Adhering to employee goals and site SOP’s
  • Must possess strong computer skills
  • Strong background in medical terminology, clinical trials or clinical research required
  • Ability to work well independently and in a team environment
  • Organized worker that can manage multiple projects
  • Excellent written and oral communication skills
  • Some travel is required
  • Two years of research experience preferred
  • RN/LPN required

Join Our Team

Don't hesitate to contact us with any questions you may have about joining the Chase Medical Research team! 

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