Clinical Research Coordinator - CEDENT

The Clinical Research Coordinator is responsible for ensuring the successful implementation, ongoing management, and performance of research studies under the medical supervision of the Principal Investigator and the Research Director. This role plays a critical part in the execution of clinical research, maintaining compliance with regulatory requirements and delivering high-quality study outcomes.
 

• Oversee the successful implementation and site management of research studies.
• Manage the performance of research studies in compliance with study protocols and under the supervision of the Principal Investigator and Research Director.
• Serve as a key liaison between clinical teams and research participants, ensuring effective communication and study coordination.

• Valid RN license in the state of employment.
• Minimum of one year of oncology or clinical research experience, or a combination of at least five years of clinical oncology and clinical research experience.
• Strong communication skills with an organized and detail-oriented approach.
• Demonstrated ability to act as a patient advocate and support the study team effectively.
• Availability to travel for investigator meetings and related activities.
• Valid driver’s license in the state of residency for clinic-related travel, with adherence to company driver safety and motor vehicle records policies.