One GI® Hiring for Clinical Research Coordinator at Louisville Metropolitan Area 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 Health Partners 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: What’s in this for you?

• 401k with match
• Tuition reimbursement
• The best swag with the coolest logo…OG
• Excellent paid time off for balance of work/life
• Internal growth opportunities with training and development
• Competitive health & supplemental benefits
• Impact somebody’s life and make a difference
• Hybrid working schedule

Snapshot of Daily Duties:

Location: 1941 Bishop Lane Louisville, KY

• 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 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.
• 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. Bachelor’s degree preferred.
• One (1) year previous experience as a clinical research coordinator for pharmaceutical phase II or III trials required.
• Previous GI trials experience preferred. Previous Research experience or equivalent experience preferred
• Clinical experience in an office or hospital setting.
• BLS certified.
• Understanding of Code of Federal Regulations for Human Subjects.
• Certified in GCP’s and HSP.
• Phlebotomy experience preferred.
• Willing to travel to New Albany location for studies.