What are the responsibilities and job description for the Clinical Research Coordinator position at Equity Medical?
Equity Medical is growing, and we are actively seeking an experienced Clinical Research Coordinator to join our new Nashville, Tennessee site.
Equity Medical is a rapidly expanding multi-site clinical research organization conducting Phase I-IV clinical trials across multiple therapeutic areas including dermatology, allergy/immunology, respiratory, rheumatology, neurology, and metabolic diseases. Our mission is to bring innovative treatment options to underserved communities through high-quality, compliant, and patient-focused clinical research operations.
We are looking for a highly organized, experienced, and proactive Clinical Research Coordinator with strong knowledge of interventional pharmaceutical-sponsored clinical trials. This is not an entry-level role. The ideal candidate will have experience independently managing studies, working directly with sponsors and CROs, and overseeing day-to-day study operations in a fast-paced clinical research environment.
Key Responsibilities:
• Coordinate and oversee all aspects of assigned clinical trials from startup through closeout
• Independently manage study visits, subject scheduling, source documentation, and data entry
• Ensure protocol compliance, GCP adherence, and regulatory compliance at all times
• Recruit, screen, and consent study participants
• Communicate directly with sponsors, CROs, monitors, investigators, and study participants
• Maintain accurate and audit-ready regulatory and study documentation
• Support monitoring visits, sponsor communication, and site operations
• Assist with study startup activities, regulatory submissions, and feasibility processes
Qualifications:
• Bachelor’s degree or equivalent combination of education and experience
• Minimum of 3 years of clinical research coordination experience preferred
• Prior experience with interventional pharmaceutical-sponsored clinical trials required
• Strong understanding of GCP, FDA regulations, and clinical trial workflows
• Experience independently managing multiple studies simultaneously
• Excellent organizational, communication, and problem-solving skills
• Ability to thrive in a growing and evolving research environment
• Strong attention to detail and ability to work both independently and collaboratively
Other Requirements:
• Direct interaction with patients and/or human research subjects
• Potential bloodborne pathogen exposure
• Completion of applicable compliance and systems training requirements
If you are passionate about clinical research and want to be part of a rapidly growing organization focused on expanding access to innovative therapies, we encourage you to apply.
Please send your CV to gulerio@equity-med.com
About Equity Medical
Equity Medical, LLC is a multi-state, multi-therapeutic clinical research organization with an independent CRO division. We are committed to fostering an inclusive, collaborative, and diverse workplace environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, veteran status, sexual orientation, gender identity, or any other protected characteristic under applicable federal or state law.