Tulane University New Orleans , LA 70130
Posted 2 weeks ago
The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases. The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols. The Clinical Research Coordinator is also responsible for keeping all data and source documentations, adverse event reporting, and IRB regulatory files.• Must be able to interact well with patients and the general public
Ability to acquire and maintain all required CITI training certificates
Ability to acquire and maintain credentialing at all required institutions
The education required for each level is listed below:
Clinical Research Coordinator I (Pay Grade 23)
OR
Clinical Research Coordinator II (Pay Grade 24)
OR
OR
Clinical Research Coordinator III (Pay Grade 25)
OR
OR
Level I
Expressed interest in Clinical Research
Motivated to learn about Clinical Research and associated regulations
Level II
Knowledge of IRB submission process and requirements
Knowledge of good clinical practices as set forth by federal regulations
Level III
Tulane University