Clinical Research Coordinator

1 week ago

New Orleans, LA, United States Tulane University Staff 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 federal and IRB regulatory policies.

  • Excellent written and verbal communication
  • Excellent computer literacy skills, including knowledge of standard office software
  • Bachelor's Degree or RN with current LA licensure at the time of hire
  • Two years clinical research experience
  • Master's degree in Public Health, Business or Social work preferred

  • Senior Clinical Research Coordinator

    1 week ago

    New Orleans, LA, United States Tulane University Staff Full time

    The primary responsibility of the Senior Clinical Research Coordinator is to manage all aspects of conducting clinical trials and other epidemiological studies related to cardiovascular disease. The Senior Clinical Research Coordinator supervises and directs the activities of workers engaged in clinical research project to ensure compliance with protocols...

  • Senior Clinical Research Coordinator

    2 weeks ago

    New Orleans, LA, United States Tulane University Staff Full time

    The primary responsibility of the Senior Clinical Research Coordinator is to manage all aspects of conducting clinical trials and other epidemiological studies related to cardiovascular disease. The Senior Clinical Research Coordinator supervises and directs the activities of workers engaged in clinical research project to ensure compliance with protocols...

  • Clinical Research Coordinator I

    3 days ago

    New Orleans, LA, United States Tulane University Staff Full time

    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...

  • Clinical Research Coordinator II

    1 week ago

    New Orleans, LA, United States Tulane University Staff 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...

  • Clinical Research Coordinator II

    2 weeks ago

    New Orleans, LA, United States Tulane University Staff 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...

  • Clinical Research Coordinator II

    8 hours ago

    New Orleans, LA, United States Tulane University Staff 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...

  • Senior Clinical Research Coordinator

    2 days ago

    New Orleans, LA, United States Medix Full time

    3-5 Must-Have Qualifications3-5 years of experience as a Lead Clinical Research Coordinator (site management experience a plus).Experience running complex protocols independently (SSU Closeout).Ability to perform all regulatory responsibilities for a study, including IRB, logs, and ISF.Full proficiency managing studies without hand-holding; cannot depend on...

  • Senior Clinical Research Coordinator

    4 days ago

    New Orleans, LA, United States Medix Full time

    3-5 Must-Have Qualifications3-5 years of experience as a Lead Clinical Research Coordinator (site management experience a plus).Experience running complex protocols independently (SSU Closeout).Ability to perform all regulatory responsibilities for a study, including IRB, logs, and ISF.Full proficiency managing studies without hand-holding; cannot depend on...

  • Senior Clinical Research Coordinator

    6 days ago

    New Orleans, LA, United States Medix Full time

    3-5 Must-Have Qualifications3-5 years of experience as a Lead Clinical Research Coordinator (site management experience a plus).Experience running complex protocols independently (SSU Closeout).Ability to perform all regulatory responsibilities for a study, including IRB, logs, and ISF.Full proficiency managing studies without hand-holding; cannot depend on...

  • Senior Clinical Research Coordinator

    7 days ago

    New Orleans, LA, United States Medix Full time

    3-5 Must-Have Qualifications3-5 years of experience as a Lead Clinical Research Coordinator (site management experience a plus).Experience running complex protocols independently (SSU Closeout).Ability to perform all regulatory responsibilities for a study, including IRB, logs, and ISF.Full proficiency managing studies without hand-holding; cannot depend on...