NGRG is seeking a Clinical Research Coordinator to independently manage significant and key aspects of clinical trials. This role oversees data management, coordinates with research participants and resolves issues related to study protocols.
CRC must have the ability to collect and assess data required by the individual protocol and reflective of the patient’s status and appropriately interpret information relative to the patient’s age-specific needs. CRC will also manage IRB submissions and respond to requests and questions, while working with study sponsors, monitors, and reporting SAEs and resolving study queries.
CRC will work in a team environment ensuring necessary staff is available to complete all portions of study visits. Ideal candidates can perform phlebotomy, specimen collection and diagnostics.
CRC’s educate potential subjects, caregivers, and referral sources on protocol specific details and expectations. Coordinate scheduled visits, adhering to protocol visit windows and timelines.
Successful candidates will be self-starters, who have the ability to multi-task, possess a strong work ethic, and have excellent attention to detail.
MINIMUM QUALIFICATIONS: Two years of college in a scientific, health related, or business administration program or Licensed as a Practical Nurse and five years of research administration experience. Candidates with a bachelor's degree in a scientific, health related or business administration and three years of research administration experience or a master's degree in a scientific field or business administration will also be considered. Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
Job Type: Full-time