Clinical Research Coordinator
3 weeks ago
Summary
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. Required Knowledge, Skills, and Abilities •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 Required Education and/or Experience The education required for each level is listed 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
Level II
•Knowledge of IRB submission process and requirements
•Knowledge of good clinical practices as set forth by federal regulations
Level III
•Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA)
•Supervisory experience Compensation Information This position is classified as "non-exempt, hourly" and is assigned to pay grade 25. Tulane offers a variety of options to enhance your health and well-being so that you may enjoy more out of life now and in the future. Learn more about as well as our Benefits and Pay. See our Candidate Resources to learn more about our hiring process and what to expect.
-
Clinical Research Coordinator
3 weeks ago
New Orleans, Louisiana, United States Tulane University Full timeClinical Research Coordinator (I, II, and III)EpidemiologyLocation: New Orleans, LASummaryThe 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...
-
Clinical Research Coordinator
1 week ago
New Orleans, Louisiana, United States Tulane University Full timeClinical Research Coordinator (I, II, and III)EpidemiologyLocation: New Orleans, LASummaryThe 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...
-
Clinical Research Coordinator
1 month ago
New Orleans, United States Tulane University Full timeCoordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating cu Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Education
-
Clinical Research Coordinator
1 month ago
New Orleans, United States Tulane University Full timeCoordinates research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening and enrolling patients in study protocols. Obtain medical histories, vital signs, and collect blood samples via veni Research Coordinator, Clinical Research, Clinical, Coordinator, Research, Healthcare, Education
-
Clinical Research Coordinator
1 month ago
New Orleans, United States Tulane University Full timeCoordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating current and future Oncology research projects. Responsible for data collection, management, and compliance with...
-
Clinical Research Coordinator, CHERISH
3 weeks ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to cardiovascular disease. The Clinical Research Coordinator assists the investigato Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Cardiovascular, Healthcare,...
-
Clinical Research Coordinator
3 weeks ago
New Orleans, United States Tulane University Full timeSummary Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating current and future Oncology research projects. Responsible for data collection, management, and...
-
Clinical Research Coordinator
1 week ago
New Orleans, United States Tulane University Full timeSummary Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating current and future Oncology research projects. Responsible for data collection, management, and...
-
Clinical Research Coordinator
1 month ago
New Orleans, United States Tulane University Full timeCoordinates research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening and enrolling patients in study protocols. Obtain medical histories, vital signs, and collect blood samples via venipuncture. Monitor patients for adverse events, compliance and progress through completion of study. Maintains...
-
Clinical Research Coordinator
1 week ago
New Orleans, United States Tulane University Full timeCoordinates research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening and enrolling patients in study protocols. Obtain medical histories, vital signs, and collect blood samples via venipuncture. Monitor patients for adverse events, compliance and progress through completion of study. Maintains...
-
Clinical Research Coordinator I
1 month ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator I is to assist in managing all aspects of conducting clinical trials. The Clinical Research Coordinator I is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As one of the primary resources for the protocol, the...
-
Clinical Research Coordinator I
1 week ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator I is to assist in managing all aspects of conducting clinical trials. The Clinical Research Coordinator I is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As one of the primary resources for the protocol, the...
-
Clinical Research Coordinator II.CRIC
6 days ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator II is to coordinate and conduct the day-to-day operation of clinical trials and other epidemiological studies. The Clinical Research Coordinator II is required to have knowledge of proto Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Education
-
Clinical Research Coordinator, CHERISH
1 month ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to cardiovascular disease. The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens,...
-
Clinical Research Coordinator, CHERISH
1 week ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to cardiovascular disease. The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens,...
-
Clinical Research Coordinator I
1 month ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator I is to assist in managing all aspects of conducting clinical trials. The Clinical Research Coordinator I is required to have an in-depth knowledge of protocol requirements and good clin Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Education
-
Clinical Research Coordinator I
1 month ago
New Orleans, United States Tulane University Full timeThe 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...
-
Clinical Research Coordinator I
2 days ago
New Orleans, United States Tulane University Full timeThe 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...
-
Clinical Research Coordinator III
3 weeks ago
New Orleans, United States Tulane University Full timeThe primary responsibility of the Clinical Research Coordinator III is to manage all aspects of conducting the NIH funded clinical study - the Precision Health Study which is led by Dr. Lu Qi, with minimal supervision. The Clinical Research Coordinat Clinical, Coordinator, Research, Healthcare, Education
-
Clinical Research Coordinator II
1 month ago
New Orleans, United States Tulane University Full timeThe Clinical Research Coordinator II will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases. The Clinical Research Coordinator II is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for protocols, the...
