Tulane University
Clinical Research Coordinator I, II & III (Covington)
Tulane University, New Orleans, Louisiana, United States, 70123
Overview
Clinical Research Coordinator I, II & III (Covington) at Tulane University. The role supports maternal health and diabetes clinical studies and trials by coordinating day-to-day operations, developing study protocols and procedures, enrolling and following participants, data collection and entry, noninvasive cardiovascular tests, and conducting small group coaching sessions. The Coordinator maintains data and source documentation, adverse event reporting, and IRB regulatory files. Responsibilities
Coordinate and conduct day-to-day operations of clinical studies and trials related to maternal health and diabetes. Assist investigator team in developing study protocols and manuals of procedures. Screen, enroll, and follow study participants; conduct data collection and entry. Perform noninvasive cardiovascular tests according to study protocols. Conduct small group coaching sessions. Maintain data and source documentation, adverse event reporting, and IRB regulatory files. Interact effectively with patients and the general public. Acquire and maintain required CITI training certificates and credentialing at required institutions. Willingness to travel to conduct clinic visits; travel to WIC clinics in Covington, Hammond, Amite, Bogalusa, Franklinton and potentially other regional locations (one location per day). Education and Experience
The education/experience requirements are listed by level below. Clinical Research Coordinator I (Pay Grade 23)
Bachelor's Degree or RN with current state licensure at the time of hire OR LPN with current state licensure at the time of hire and three (3) years of related work experience Clinical Research Coordinator II (Pay Grade 24)
Bachelor's Degree or RN with current state licensure at the time of hire and one (1) year of related work experience OR LPN with current state licensure at the time of hire and four (4) years of related work experience OR Master\'s Degree in a related field Clinical Research Coordinator III (Pay Grade 25)
Bachelor's Degree or RN with current state licensure at the time of hire and two (2) years of related work experience OR LPN with current state licensure at the time of hire and five (5) years of related work experience OR Master\'s Degree and one (1) year of related work experience Preferred Qualifications
Level I
Expressed interest in Clinical Research Motivated to learn about Clinical Research and associated regulations Preferred Spanish language fluency—oral and written Level II
Knowledge of IRB submission process and requirements Knowledge of good clinical practices as set forth by federal regulations Preferred Spanish language fluency—oral and written Level III
Certification as a Certified Clinical Research Coordinator (CCRC/ACRP) or Certified Clinical Research Professional (CCRP/SoCRA) Supervisory experience Preferred Spanish language fluency—oral and written Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Higher Education
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Clinical Research Coordinator I, II & III (Covington) at Tulane University. The role supports maternal health and diabetes clinical studies and trials by coordinating day-to-day operations, developing study protocols and procedures, enrolling and following participants, data collection and entry, noninvasive cardiovascular tests, and conducting small group coaching sessions. The Coordinator maintains data and source documentation, adverse event reporting, and IRB regulatory files. Responsibilities
Coordinate and conduct day-to-day operations of clinical studies and trials related to maternal health and diabetes. Assist investigator team in developing study protocols and manuals of procedures. Screen, enroll, and follow study participants; conduct data collection and entry. Perform noninvasive cardiovascular tests according to study protocols. Conduct small group coaching sessions. Maintain data and source documentation, adverse event reporting, and IRB regulatory files. Interact effectively with patients and the general public. Acquire and maintain required CITI training certificates and credentialing at required institutions. Willingness to travel to conduct clinic visits; travel to WIC clinics in Covington, Hammond, Amite, Bogalusa, Franklinton and potentially other regional locations (one location per day). Education and Experience
The education/experience requirements are listed by level below. Clinical Research Coordinator I (Pay Grade 23)
Bachelor's Degree or RN with current state licensure at the time of hire OR LPN with current state licensure at the time of hire and three (3) years of related work experience Clinical Research Coordinator II (Pay Grade 24)
Bachelor's Degree or RN with current state licensure at the time of hire and one (1) year of related work experience OR LPN with current state licensure at the time of hire and four (4) years of related work experience OR Master\'s Degree in a related field Clinical Research Coordinator III (Pay Grade 25)
Bachelor's Degree or RN with current state licensure at the time of hire and two (2) years of related work experience OR LPN with current state licensure at the time of hire and five (5) years of related work experience OR Master\'s Degree and one (1) year of related work experience Preferred Qualifications
Level I
Expressed interest in Clinical Research Motivated to learn about Clinical Research and associated regulations Preferred Spanish language fluency—oral and written Level II
Knowledge of IRB submission process and requirements Knowledge of good clinical practices as set forth by federal regulations Preferred Spanish language fluency—oral and written Level III
Certification as a Certified Clinical Research Coordinator (CCRC/ACRP) or Certified Clinical Research Professional (CCRP/SoCRA) Supervisory experience Preferred Spanish language fluency—oral and written Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Higher Education
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