Clinical Research Coordinator

Equity Medical LLC.; Nashville (TN); Presencial; USD 60.000 - 80.000; Jornada completa

Descripción de la vacante

Equity Medical LLC. is seeking an experienced Clinical Research Coordinator for our Nashville, Tennessee site. We conduct Phase I-IV trials across dermatology, allergy/immunology, respiratory, rheumatology, neurology and metabolic diseases.

The role requires 3+ years of coordination experience, knowledge of interventional trials, and a strong grasp of GCP and FDA regulations. You will manage multiple studies, interact with sponsors and CROs, and oversee day-to-day site operations.

Formación

• Bachelor's degree or equivalent required.
• 3+ years clinical research coordination experience preferred.
• Interventional pharmaceutical-sponsored trials experience required.
• Strong knowledge of GCP and FDA regulations.
• Experience managing multiple studies independently.

Responsabilidades

• Coordinate all aspects of assigned trials from startup through closeout.
• Independently manage visits, scheduling, source docs, and data entry.
• Ensure protocol compliance, GCP and regulatory adherence.
• Recruit, screen, and consent participants.
• Communicate with sponsors, CROs, monitors, investigators, and participants.
• Maintain audit-ready regulatory and study documentation.
• Support monitoring visits and sponsor communications.
• Assist with startup activities and regulatory submissions.

Conocimientos

Interventional trials experience

Study coordination

Regulatory compliance

Data entry / source documentation

Communication skills

Organizational skills

Educación

Bachelor's degree or equivalent

Descripción del empleo

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
• Completion of applicable compliance and systems training requirements

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.