Clinical Research Coordinator

Job Details

Are you looking for a rewarding career where you can grow your skillset and make a real impact in the field of healthcare? Do you want to work in an inclusive environment where innovation and patient care come first?

At Gastroenterology Health Partners we are dedicated to advancing digestive health through cutting-edge research and exceptional patient care.  We are currently seeking a Clinical Research Coordinator to join our team in Louisville, KY – a vibrant city with a strong medical community and opportunities for professional development.

Discover the Amazing Benefits We Offer: 

• Excellent paid time off for a healthy work/life balance.
• We want to help you with your retirement, with our generous 401k plan. We will match 100% of the first 3% that you contribute, and 50% of the next 2% of your eligible contributions.
• Looking to further your education, we want to help! We offer education reimbursement, up to $10,000 per year (depending on employment status).
• Internal growth opportunities. We want to aide in your training and development.
• Competitive health and supplemental benefits; with FSA and HSA options.
• 100% Employer paid Short Term and Long Term Disability Insurance. 
• After landing your job, why not bring a friend on board? Refer someone you know to One GI®, and not only will they get a fantastic opportunity, but you'll also score a cool $500 referral bonus. It's a win-win!

Why Join Us?

• Shape the Future of healthcare – Be at the forefront of groundbreaking clinical research that improves patient outcomes
• Collaborate with Experts – Work alongside leading gastroenterologists, healthcare professionals, and research specialists.
• Thrive in Supportive Environment – We champion inclusivity and teamwork, ensuring you feel valued and empowered in our role.
• Impact Lives -  Your contributions will help advance treatments for digestive diseases and enhance patient care.

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.
• 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:

• 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. Phlebotomy experience preferred.
• Previous Research experience or equivalent experience preferred
• BLS certified.
• Understanding of Code of Federal Regulations for Human Subjects.
• Certified in GCP’s and HSP preferred, will obtain certifications during training.
• Travel to our Louisville/New Albany office locations