Careers at Equity Medical

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.

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