Join to apply for the Clinical Research Coordinator role at One GI
Are you looking for a rewarding career where you can grow your skillset and make a real impact in healthcare? Do you want to work in an inclusive environment where innovation and patient care come first?
At Dayton Gastroenterology, 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 Englewood, OH – a 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.
- Generous 401k plan with matching: 100% of the first 3%, and 50% of the next 2% of contributions.
- Education reimbursement up to $10,000 per year (depending on employment status).
- Internal growth opportunities and support for training and development.
- Competitive health and supplemental benefits, including FSA and HSA options.
- 100% employer-paid Short Term and Long Term Disability Insurance.
- Referral bonus: $500 for referring a friend who joins our team.
Why Join Us?
- Shape the future of healthcare through groundbreaking clinical research.
- Collaborate with leading gastroenterologists, healthcare professionals, and research specialists.
- Work in a supportive, inclusive, and team-oriented environment.
- Contribute to advancing treatments for digestive diseases and improving patient care.
Snapshot Of Daily Duties
- Manage industry-sponsored clinical trials administratively and clinically.
- Assist in patient recruitment via chart reviews and interviews.
- Discuss study protocols and verify informed consent documentation.
- Review patient medical histories against study criteria.
- Perform blood draws, process and ship specimens per protocol and regulations.
- Schedule research visits and procedures.
- Dispense study medication, record vital signs, perform ECGs.
- Maintain case report forms per FDA guidelines, review for accuracy.
- Monitor patients and coordinate with medical staff for optimal outcomes.
- Educate patients about their disease and study participation.
- Assist with administrative tasks related to research operations.
- Facilitate clinical trials from start to finish.
The Must Haves
- At least 1 year of experience as a clinical research coordinator in phase II or III trials.
- Clinical experience in an office or hospital setting; phlebotomy preferred.
- Research experience or equivalent preferred.
- BLS certification.
- Understanding of CFR for Human Subjects.
- GCP and HSP certification preferred; training provided if needed.
- Willingness to travel to Beavercreek locations.