Clinical Research Coordinator

ith their skills, goals, and passions.

Job Overview:
FOCUSPOINT is seeking experienced Clinical Research Coordinators for multiple client sites across Texas, Virginia, and Florida.

This role is ideal for professionals with a strong interest in clinical research and a desire to grow their knowledge of research operations and regulations. You’ll play a key role in coordinating multiple research protocols, acting as a liaison between site personnel, investigators, and sponsors.

Schedule: Monday–Friday, 7:00 AM to 4:00 PM (Hours may be adjusted by the Hiring Division Director)

Key Responsibilities:
• Coordinate routine operational activities across multiple research protocols
• Serve as a liaison between research site staff, sponsors, and supervisors
• Collaborate with internal departments including finance and compliance teams
• Manage study timelines from feasibility through study closeout
• Review study criteria with physicians and patients; ensure informed consent procedures are followed
• Maintain data accuracy in case report forms and electronic systems
• Track shipments of drugs, devices, and supplies
• Monitor and report adverse events and protocol deviations
• Attend site meetings, investigator calls, and training sessions
• Respond to audits and monitoring findings

Qualifications:
• Bachelor’s degree required
• 1+ year of relevant clinical research experience or equivalent combination of education and experience
• Certified Clinical Research Coordinator (preferred)
• Basic understanding of medical terminology and ICH/GCP guidelines
• Strong communication and organizational skills
• Ability to perform clinical procedures including ECG acquisition, phlebotomy, and specimen processing (training provided as needed)
• Self-motivated with excellent attention to detail
• Occasional travel may be required

Benefits:
• Dental insurance
• Health insurance
• Health savings account
• Life insurance
• Vision insurance