Research Coordinator

About the role

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

Key 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.

What We're Looking For

• Detail-Oriented & Organized
• Able to manage multiple priorities while maintaining a high level of accuracy and quality.
• Strong Communicator
• Effectively communicates with sponsors, investigators, site staff, and participants.
• Collaborative Team Player
• Works well independently and as part of a multidisciplinary team.
• Adaptable & Results-Oriented
• Thrives in a dynamic environment and remains focused on achieving study goals.

Experience & 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.
• Experience with electronic data capture systems and regulatory documentation preferred.

Why CVAUSA?

We believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As part of our growing organization, you'll be at the forefront of cutting-edge clinical trials.