Clinical Research Coordinator

About Us

Our organization places patients at the center, uniting clinical experts, therapeutic area specialists, and biopharmaceutical companies to propel medical science. We emphasize conducting clinical trials that are quicker, more effective, and of superior quality. Our goal is to close the gap between research and patient care, fostering enhanced outcomes. Through collaboration and innovation, we are dedicated to advancing scientific discoveries.

Role Overview

This full-time, on-premise position requires a Clinical Research Coordinator responsible for managing clinical research trials in compliance with established protocols and relevant regulations. The role involves obtaining informed consent from study participants, liaising closely with investigators regarding study procedures, coordinating daily clinical trial activities, and ensuring meticulous documentation of research data and records. Coordinators will collaborate with cross-disciplinary teams and monitor study progress to promote quality and operational efficiency. Assignment to specific sites is expected, with on-site presence as required.

Qualifications and Requirements

• At least one year of clinical research experience is necessary.
• Expertise in securing informed consent and comprehensive knowledge of protocol directives.
• Proven background in research and clinical research principles.
• Direct experience conducting clinical trials and familiarity with their related workflows.
• Excellent organizational capabilities paired with strong communication skills.
• Commitment to adhering to regulatory standards and ethical practices.
• A bachelor's degree in a pertinent field or comparable practical experience is essential.
• Certification in clinical research coordination is advantageous.