Research Coordinator Jobs

About The Position

Requirements

• Clinical experience in cardiovascular medicine in a licensed role, such as RN, technologist, or medical assistant.
• Minimum of 1–2 years of clinical research experience, including patient enrollment and study coordination.
• Strong organizational and time management skills.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Ability to manage multiple priorities while maintaining accuracy and quality.
• Strong communication skills with sponsors, investigators, site staff, and participants.
• Ability to work independently and as part of a multidisciplinary team.
• Adaptability and focus on achieving study goals in a dynamic environment.

Nice To Haves

• Bachelor’s degree in a relevant field, such as life sciences, healthcare, or clinical research.
• Clinical research certification, such as CCRP.
• Experience with electronic data capture systems and regulatory documentation.

Responsibilities

• Coordinate clinical trial activities, including patient recruitment, screening, enrollment, and follow-up visits, and ensure study protocols are followed accurately and consistently.
• Support day-to-day research site operations while ensuring compliance with regulatory requirements and study protocols.
• Collect, verify, and maintain clinical trial data, ensuring accuracy, completeness, and timely entry.
• Serve as a primary point of contact for study sponsors, participants, and research stakeholders.
• Provide regular study updates and assist with reporting requirements.
• Maintain current study documentation, regulatory binders, and patient records in compliance with GCP, ICH guidelines, and applicable regulations.
• Identify opportunities to improve research workflows and enhance study performance.