Clinical Research Assistant Opportunities – Multiple Locations Nationwide

Headlands Research • Lake Worth, FL

6d • Onsite

About The Position

This general interest posting is designed for Clinical Research Assistants (RAs) 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. Research Assistants play a critical role in supporting clinical trials and bridging the gap between research and patient care. This is an ideal opportunity for individuals with patient-care, lab, academic, or research experience who are looking to transition into a clinical research role and gain hands-on clinical exposure. When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for current and upcoming Research Assistant 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. Research Assistants support the execution of clinical trials by assisting with study visits, preparing study materials, collecting and organizing data, and helping ensure studies run smoothly and in compliance with protocols. This role offers direct exposure to patient interactions, clinical workflows, and regulatory processes. Research Assistants work closely with Clinical Research Coordinators, investigators, and patients, gaining valuable experience that can serve as a strong foundation for advancement into Clinical Research Coordinator roles and beyond. Responsibilities may vary depending on experience level and site needs but are designed to provide meaningful, hands-on learning and growth opportunities.

Requirements

• A bachelor’s or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar)
• Hands-on experience in lab work, research projects, or clinical environments
• Strong attention to detail and the ability to follow structured protocols
• Excellent organizational and time management skills
• Clear communication skills and a desire to work directly with patients and care teams
• A positive team-based attitude and approach

Nice To Haves

• Prior clinical research experience is a plus

Responsibilities

• Assisting with study visits
• Preparing study materials
• Collecting and organizing data
• Helping ensure studies run smoothly and in compliance with protocols

Benefits

• A strong entry point into clinical research with exposure to both research and patient care
• Hands-on experience supporting clinical trials and working alongside experienced CRCs and investigators
• Opportunities to learn Good Clinical Practice (GCP), regulatory processes, and study operations
• Clear pathways for growth into Clinical Research Coordinator and other roles
• The opportunity to contribute to developing new treatments that improve patient outcomes

What This Job Offers

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