Clinical Research Coordinator

Clinical Research Coordinator (CRC)

Location: Florida - (Two different locations to choose)

Employment Type: Full-Time

Industry: Clinical Research

About the Opportunity

A growing and well-established clinical research organization is seeking an experienced Clinical Research Coordinator (CRC) to join their team. This individual will play a key role in supporting Phase I–IV clinical trials by managing study operations, ensuring protocol compliance, and providing high-quality patient care throughout the research process.

This is an excellent opportunity to join a collaborative team environment with strong leadership and continued growth.

Key Responsibilities

• Coordinate and manage clinical trials in accordance with protocol, GCP, and regulatory requirements
• Screen and recruit study participants, including reviewing medical history and determining eligibility
• Schedule and conduct subject visits, including collecting vitals and performing study-related procedures
• Maintain accurate source documentation and ensure timely data entry into EDC and CTMS systems
• Communicate effectively with Principal Investigators, Sponsors, CROs, and study team members
• Assist with query resolution and monitor/audit preparation
• Process and ship laboratory specimens per protocol requirements
• Maintain investigational product accountability and documentation
• Educate study participants and provide ongoing support throughout the trial
• Identify and escalate protocol deviations or operational challenges

Recruitment & Study Support

• Support recruitment initiatives and collaborate with internal recruitment teams
• Provide regular enrollment updates and participate in study start-up activities
• Assist with study materials, patient outreach, and retention strategies

Qualifications

• Minimum 2+ years of Clinical Research Coordinator experience
• Experience working on industry-sponsored clinical trials preferred
• Knowledge of FDA regulations, ICH-GCP, and clinical trial processes
• Phlebotomy, ECG, and patient-facing clinical skills preferred
• CCRC or CCRP certification is a plus

Skills & Competencies

• Strong organizational and multitasking abilities
• Excellent communication and interpersonal skills
• Detail-oriented with strong documentation practices
• Ability to work independently and within a team environment
• Comfortable working in a fast-paced clinical research setting
• Proficiency with EDC, CTMS, and Microsoft Office

Why Apply?

• Opportunity to join a reputable and growing research organization
• Collaborative and supportive team environment
• Competitive compensation package
• Career growth and development opportunities