Clinical Research Coordinator

3 weeks ago

Memphis, United States One GI® Full time

Have you been looking for a place to grow your skillset? Or perhaps you are looking for a place to develop your career surrounded by a diverse group where employees feel a sense of belonging.


At Gastro One we are championing the power of inclusivity and a people first mentality. We hope to improve the human experience – from our patients to our colleagues.


If you are interested in joining our culture, we’re looking for a Clinical Research Coordinator.

The Perks

  • 401k with match
  • Tuition reimbursement
  • Competitive health & supplemental benefits
  • Excellent paid time off for balance of work/life.
  • Internal growth opportunities with training and development.


Snapshot of Daily Duties

  • Administratively and clinically manage industry sponsored clinical trials.
  • Assist in patient recruitment by performing detailed chart reviews and patient interviews
  • Discuss study protocols with patients and verify the informed consent documentation.
  • Review medical history of patient against inclusion/exclusion criteria of studies.
  • Perform blood draws, process and ship blood/urine specimens per study protocol and IATA regulations.
  • Schedule all patient research visits and procedures consistent with protocol requirements
  • Dispense study medication, collect vital signs, and perform ECGs.
  • Complete and maintain case report forms per FDA guidelines and review them against the patient’s medical record for completeness and accuracy.
  • Monitor patients and providing information to the medical staff and other staff members to assure optimal outcomes.
  • Coordinate the availability and distribution of medications for patients in a timely manner.
  • Responsible for the education of patients in all aspects of the disease process and/or clinical study in which the patient may be involved.
  • Assist the principal investigator and research director with various administrative tasks associated with the day-to-day operations of research studies and projects.
  • Facilitate assigned clinical trial from start to finish.

The Must Haves

  • Associate Degree in a clinical or scientific related discipline required. Bachelors preferred
  • One (1) year previous experience as a clinical research coordinator for pharmaceutical phase II or III trials required.
  • Clinical experience in an office or hospital setting.
  • Research experience or equivalent.
  • BLS certified.
  • Understanding of Code of Federal Regulations for Human Subjects.
  • Certified in GCP’s and HSP.
  • Phlebotomy experience preferred.

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