What are the responsibilities and job description for the Clinical Research Coordinator position at Discover International?
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