Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide

Benefits

Qualifications

• •A bachelor’s degree in a scientific or healthcare‑related field (e.g., biology, chemistry, psychology, pre‑med, or similar) and/or
• •Hands‑on experience in lab courses, research projects, or clinical settings (internships, volunteering, or academic labs)
• •Strong attention to detail and the ability to follow structured protocols
• •Excellent organizational and time‑management skills
• •Clear communication skills and comfort interacting with patients and team members
• •A genuine interest in healthcare, research, or improving patient outcomes
• •Prior experience as a CRC is required for some locations
• •Hands‑on experience working with patients and clinical trial protocols
• •Opportunities to learn GCP, regulatory processes, and study operations
• •6 more items(s)

Responsibilities

• •Clinical Research Coordinators support the day‑to‑day execution of clinical trials
• •This includes working directly with patients, coordinating study visits, collecting and managing data, and ensuring studies are conducted in compliance with protocols and regulatory requirements
• •CRCs work closely with investigators, patients, and cross‑functional teams, gaining exposure to a wide range of therapeutic areas and research processes
• •Roles may vary based on experience level and site needs, with opportunities to grow and take on increasing responsibility over time
• •Clear pathways for growth into CRC II, III, and senior, regulatory, or leadership roles
• •The chance to contribute to the development of new treatments that impact patients’ lives
• •3 more items(s)