Job Details
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.