Ophthalmic Clinical Research Coordinator

Overview
Join our dynamic clinical research team as a Clinical Research Coordinator, a pivotal role dedicated to advancing medical knowledge through meticulous management of clinical trials. In this energetic position, you will coordinate all aspects of clinical studies, ensuring compliance with regulatory standards and maintaining the highest quality data collection. Your proactive approach will support the development of innovative therapies and improve patient outcomes, making a tangible difference in healthcare. This paid position offers an exciting opportunity to grow your expertise in clinical research within a collaborative and forward-thinking environment.

Duties

• Oversee the daily operations of clinical trials, including participant recruitment, enrollment, and retention strategies.
• Manage documentation review to ensure accuracy, completeness, and regulatory compliance across all trial records.
• Monitor patient progress by collecting vital signs, blood samples through phlebotomy, and tracking adverse events or protocol deviations.
• Coordinate with clinical laboratories to facilitate sample processing and ensure timely reporting of results.
• Maintain detailed records using electronic medical record (EMR) systems and adhere to HIPAA regulations to protect patient confidentiality.
• Ensure adherence to FDA regulations, ICH Good Clinical Practice (GCP) guidelines, and CDISC standards for data management and reporting.
• Supervise research staff and volunteers, providing guidance on clinical trials management and compliance procedures.

Skills

• Proven experience in a clinical research an ophthamology setting.
• Strong knowledge of clinical trials management.
• Proficiency in medical terminology, data collection methods, and analysis skills relevant to clinical development.
• Experience with EMR systems, and data management tools aligned with research protocols.
• Familiarity with HIPAA regulations, FDA guidelines, ICH GCP certification from a recognized issuer for CA (California).
• Clinical laboratory experience including blood sampling (phlebotomy), vital signs measurement, and sample handling procedures.
• Excellent organizational skills with the ability to manage multiple studies simultaneously while maintaining compliance management protocols. Embark on a rewarding career where your expertise fuels groundbreaking research! We are committed to fostering an inclusive environment that values your growth as a professional dedicated to advancing healthcare through rigorous clinical trial management.

Pay: $21.00 - $30.17 per hour

Work Location: In person