Clinical 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 with accuracy and quality.
• Strong communication skills with sponsors, investigators, site staff, and participants.
• Ability to work independently and as part of a multidisciplinary team.
• Ability to adapt in a dynamic environment and remain focused on study goals.

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 trials, 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 and ensure 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.
• Help identify opportunities to improve research workflows and study performance.