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

Headlands Research • Lake Worth, FL

10h • Remote

About The Position

This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. Clinical Research Coordinators are at the heart of our work. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care. When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for current and upcoming CRC opportunities. As new roles open, we proactively match candidates based on location preference, education, experience, and career interests. If there’s a strong fit, a member of our team will reach out to start the conversation. 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.

Requirements

• 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

Responsibilities

• Support the day-to-day execution of clinical trials.
• Work directly with patients.
• Coordinate study visits.
• Collect and manage data.
• Ensure studies are conducted in compliance with protocols and regulatory requirements.
• Work closely with investigators, patients, and cross-functional teams.

Benefits

• A strong entry point into the clinical research and healthcare industry
• Hands-on experience working with patients and clinical trial protocols
• Opportunities to learn GCP, regulatory processes, and study operations
• Mentorship and training to help you build a long-term career in research
• Clear pathways for growth into CRCII, III, and senior, regulatory, or leadership roles
• The chance to contribute to the development of new treatments that impact patients’ lives

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 11-50 employees