Clinical Research Coordinator
About The Position
DelRicht Research is seeking a Clinical Research Coordinator who is excited about patient care and clinical research. The role focuses on providing excellent patient care and a positive experience for participants in clinical research studies. The coordinator supports patient screening, enrollment, and retention; guides patients through study requirements; completes visits accurately and efficiently while adhering to trial protocols and site expectations; enters clinical data into required systems; and communicates clearly with patients, physicians, and other stakeholders. Candidates should be comfortable performing clinical skills such as blood draws, EKGs, vital signs, and charting; training is provided. Previous research experience is not required. The position is full-time, with a schedule of 8 a.m. to 5 p.m., Monday through Friday, and is on-site at two clinics in Hendersonville and Smyrna, Tennessee. The base salary is $60,000–$65,000. Quarterly bonuses may bring estimated annual earnings to $66,000–$75,000, depending on performance and productivity; bonuses are not guaranteed.
Requirements
- At least 1 year of professional experience, ideally in a medical or clinical environment.
- Strong communication skills, sound judgment, and a decisive, solutions-oriented approach to fast-moving or uncertain situations.
- High attention to detail and the ability to stay organized across competing priorities.
- Ability to quickly learn protocols, systems, and clinical workflows.
- Collaborative, patient-focused mindset.
- Comfort performing clinical skills such as blood draws, EKGs, vital signs, and charting; training is provided.
Nice To Haves
- Bachelor's degree from an accredited college or university.
- Experience in customer service, healthcare, sales, hospitality, or another fast-paced professional environment.
Responsibilities
- Provide quality patient care and create a positive, comfortable patient experience throughout clinical research studies.
- Complete patient visits accurately and efficiently, adhering to clinical trial protocols and site expectations.
- Execute patient screening, enrollment, and retention activities with attention to safety, accuracy, and timely follow-through.
- Guide patients through the study journey and help ensure they attend and complete required visits.
- Enter clinical data accurately and on time into required systems and platforms.
- Communicate clearly and promptly with patients, physicians, and other stakeholders.
- Perform clinical skills during patient visits, including blood draws, EKGs, vital signs, and charting.
Benefits
- Medical insurance with generous employer-paid contributions.
- Dental and vision insurance.
- Short- and long-term disability coverage.
- Group life coverage.
- Paid time off that builds throughout a career with the company.
- 401(k) with discretionary match or profit sharing.
- Quarterly bonus plan.
- Professional development program.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
