Clinical Research Coordinator I
Tulane University
New Orleans, LA
Full-time
Research
Posted on November 16, 2023
This is an entry-level coordinator position. Training will be provided to develop the necessary skills required of a clinical research coordinator. The primary responsibility of the Clinical Research Coordinator I is to conduct the day-to-day study visits for clinical trials and other epidemiological studies. The Clinical Research Coordinator I will be trained to follow study protocol and good clinical practices for all study visits. The Clinical Research Coordinator I will screen and enroll study participants, arrange study visits, and perform retention and follow-up activities. The Clinical Research Coordinator I will conduct data collection and entry and performs physical examinations and laboratory tests according to study protocols. These are all part of the learning process required in this primary position for advancement towards a Clinical Research Coordinator II and Clinical Research Coordinator III position. The Clinical Research Coordinator I assists with all data and source documentation, adverse event reporting and maintenance of complete regulatory files, also as a part of the learning experience.
Your Privacy Choices