Clinical Research Coordinator

2 weeks ago

East Canton, 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 Gastroenterology & Hepatology Specialists, INC, 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, were looking for a full-time Clinical Research Coordinator in our Research Center located at 4360 N Fulton Drive Canton, OH

The Perks: What's in it for you?

  • 401k with match
  • Tuition reimbursement
  • The best swag with the coolest logoOG
  • Excellent paid time off for balance of work/life
  • Internal growth opportunities with training and development
  • Competitive health & supplemental benefits
  • Impact somebodys life and make a difference

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 patients medical record for completeness and accuracy.
  • Maintain compliance of protocols and regulatory guidelines for studies performed in the research area.
  • Perform phlebotomy for lab work as required and completes all necessary forms.
  • Monitor the progress of research activities; develop and maintain records of research activities, and prepare periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies.
  • Triage phone calls from subjects, be able to answer clinical care questions within the scope of practice; determine when escalation is required.

Must Haves:

  • Associates degree in a clinical or scientific related discipline required. Bachelor's degree is preferred.
  • One (1) year previous experience as a clinical research coordinator for pharmaceutical phase II or III trials required.
  • Must maintain current licensure and/or certification.
  • BLS certified.
  • Understanding of clinical research documentation standards.
  • Working knowledge of industry standards and regulatory requirements relevant to clinical drug trails.
  • Understanding of Code of Federal Regulations for Human Subjects.
  • Certified in GCPs and HSP.
  • Periodic local travel to other practice locations on an as-needed basis.
  • Phlebotomy experience preferred.

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