Clinical Research Coordinator, MH-CIP

3 weeks ago


New Orleans, United States Tulane University Full time

The 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 maternal health and diabetes. 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 documentation, 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)

* Licensed Practical Nurse with current state licensure at the time of hire and 3 years of related work experience

OR

* Bachelor's Degree or Registered Nurse with current state licensure at the time of hire

Clinical Research Coordinator II (Pay Grade 24)

* Licensed Practical Nurse with current state licensure at the time of hire and 4 years of related work experience

OR

* Bachelor's Degree or Registered Nurse with current state licensure at the time of hire and 1 year of related work experience

OR

* Master's Degree in a related field

Clinical Research Coordinator III (Pay Grade 25)

* Licensed Practical Nurse with current state licensure at the time of hire and 5 years of related work experience

OR

* Bachelor's Degree or Registered Nurse with current state licensure at the time of hire and 2 years of related work experience

OR

* Master's Degree in a related field and 1 year of related experience

FOR ALL LEVELS: Spanish language fluency-oral and written

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



  • New Orleans, Louisiana, United States Tulane University Full time

    Clinical 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...


  • New Orleans, Louisiana, United States Tulane University Full time

    Clinical 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...


  • New Orleans, United States Tulane University Full time

    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 cu Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Education


  • New Orleans, United States Tulane University Full time

    Coordinates 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


  • New Orleans, United States Tulane University Full time

    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 compliance with...


  • New Orleans, United States Tulane University Full time

    The 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,...


  • New Orleans, United States Tulane University Full time

    Summary 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...


  • New Orleans, United States Tulane University Full time

    Summary 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...


  • New Orleans, United States Tulane University Full time

    Coordinates 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...


  • New Orleans, United States Tulane University Full time

    Coordinates 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...


  • New Orleans, United States Tulane University Full time

    The 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...


  • New Orleans, United States Tulane University Full time

    The 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...


  • New Orleans, United States Tulane University Full time

    The 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


  • New Orleans, United States Tulane University Full time

    The 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,...


  • New Orleans, United States Tulane University Full time

    The 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,...


  • New Orleans, United States Tulane University Full time

    The 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


  • New Orleans, United States Tulane University Full time

    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...


  • New Orleans, United States Tulane University Full time

    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...


  • New Orleans, United States Tulane University Full time

    The 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


  • New Orleans, United States Tulane University Full time

    The 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...