Research Coordinator

About the role

The Clinical Research Coordinator will play a key role in coordinating and overseeing clinical trials and supporting site operations. They will manage studies with a high degree of autonomy while working closely with investigators, sponsors, and site staff.

Responsibilities

• Clinical Trial Coordination
• Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits.
• Ensure study protocols are followed accurately and consistently.
• Site Operations
• Support day-to-day research site operations while ensuring compliance with regulatory requirements and study protocols.
• Data Management
• Collect, verify, and maintain clinical trial data, ensuring accuracy, completeness, and timely entry.
• Communication & Reporting
• Serve as a primary point of contact for study sponsors, participants, and research stakeholders.
• Provide regular study updates and assist with reporting requirements.
• Regulatory Compliance
• Maintain up-to-date study documentation, regulatory binders, and patient records in compliance with GCP, ICH guidelines, and applicable regulations.
• Process Improvement
• Assist with identifying opportunities to improve research workflows and enhance study performance.

Requirements

• Detail-Oriented & Organized
• Strong Communicator
• Collaborative Team Player
• Adaptable & Results-Oriented

Qualifications

• Minimum of 1–2 years of clinical research experience, including patient enrollment and study coordination.
• Strong organizational and time management skills.
• Preferred: Bachelor’s degree in a relevant field (life sciences, healthcare, or clinical research).
• Preferred: Clinical research certification (e.g., CCRP).
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Preferred: Experience with electronic data capture systems and regulatory documentation.