Clinical Research Coordinator - Memphis, United States - One GI

Description

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, were 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 patients 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 GCPs and HSP.
• Phlebotomy experience preferred.