Clinical Research Coordinator II.CRIC

2 months ago


New Orleans, United States Tulane University Full time

Summary

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 protocol requirements and good clinical practices as set forth by federal regulations. The Clinical Research Coordinator II is able to recruit, follow, and retain study participants, and perform study visits, data collection and entry, and quality control activities according to study protocol independently. The Clinical Research Coordinator II is also able to perform procedures required by the study protocol(s), such as blood pressure measurements, EKD, and laboratory processing. The Clinical Research Coordinator II is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files, under direct supervision. Required Knowledge, Skills, and Abilities •Knowledge of good clinical research practice is required
•Must be able to interact well with patients and the general public
•Excellent organization, analytical, interpersonal, and communication skills
•Ability to maintain confidentiality in all work performed
•Proficient in various software programs (including database management [e.g. Access], presentation packages [e.g. PowerPoint], spreadsheets [e.g. Excel], and advanced word processing [e.g. Word]).
•Ability to acquire and maintain all required CITI training certificates
•Ability to acquire and maintain credentialing at all required institutions: Tulane Medical Center, Veterans Administration Hospital/New Orleans, LA and University Medical Center.

REQUIRED BACKGROUND CHECK, PHYSICAL, AND DRUG SCREENING FOR INCUMBENTS WHO HAVE CONTACT OR EXPOSURE TO ANIMALS OR ANIMAL TISSUES:
Selected candidates must complete and pass a background check and an occupational health screening as a condition of employment. For identified jobs, a drug screening will also be required. The background investigation, required occupational health screening, and any required drug screening will be conducted after a conditional employment offer has been extended. Required Education and/or Experience •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
•A Master’s Degree in a related field Preferred Qualifications •Knowledge of IRB submission process and requirements. •Knowledge of good clinical practices as set forth by federal regulations. Compensation Information This position is classified as "non-exempt, hourly" and is assigned to pay grade 24. 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.

  • New York, United States Brooklyn Clinical Research Full time

    Clinical Research CoordinatorLocation: Brooklyn, NYCompany history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical-trial enrollment should accurately represent the broader population. In meeting this objective, we help improve therapeutic efficacy and safety for all individuals.This...


  • New York, United States Brooklyn Clinical Research Full time

    Clinical Research CoordinatorLocation: Brooklyn, NYCompany history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical-trial enrollment should accurately represent the broader population. In meeting this objective, we help improve therapeutic efficacy and safety for all individuals.This...


  • New York, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinic Research Coordinator II The Clinical Research Coordinator II, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study...


  • New York, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinic Research Coordinator II The Clinical Research Coordinator II, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study...


  • New York, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinic Research Coordinator II The Clinical Research Coordinator II, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study...


  • New York, United States Brooklyn Clinical Research Full time

    Location: Brooklyn, NY (Flatbush)Job Type: Full-timeCompany History: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical-trial enrollment should accurately represent the broader population. To support this objective, we establish clinical research sites in densely populated metropolitan...


  • New York, United States Brooklyn Clinical Research Full time

    Location: Brooklyn, NY (Flatbush)Job Type: Full-timeCompany History: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical-trial enrollment should accurately represent the broader population. To support this objective, we establish clinical research sites in densely populated metropolitan...


  • New York, United States Manhattan Research Clinical Site Midtown Full time

    Clinical Research Coordinator PositionManhattan Psychiatry Research Practice is looking for someone who is professional, friendly, motivated, and hard working. Prior clinical or patient experience is required.Qualified applicants will:•   Be organized and exhibit high attention to detail.•   Be able to multi-task•   Have a professional,...


  • New York, United States Manhattan Research Clinical Site Midtown Full time

    Clinical Research Coordinator PositionManhattan Psychiatry Research Practice is looking for someone who is professional, friendly, motivated, and hard working. Prior clinical or patient experience is required.Qualified applicants will:•   Be organized and exhibit high attention to detail.•   Be able to multi-task•   Have a professional,...


  • New York, United States Manhattan Research Clinical Site Midtown Full time

    Clinical Research Coordinator PositionManhattan Psychiatry Research Practice is looking for someone who is professional, friendly, motivated, and hard working. Prior clinical or patient experience is required.Qualified applicants will:•   Be organized and exhibit high attention to detail.•   Be able to multi-task•   Have a professional,...


  • 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 an Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Education


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

    Clinical Research Coordinator I, II & III (Thibodaux)EpidemiologyLocation: Houma, LASummaryThe 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...


  • New Orleans, United States Tulane University Full time

    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...


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


  • New Orleans, United States Tulane University Full time

    Clinical Research Coordinator I, II & III (Thibodaux)EpidemiologyLocation: Houma, LASummaryThe 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...


  • New York, United States NYU Langone Health Full time

    We have an exciting opportunity to join our team as a Clinical Research Coordinator. The Oncology Clinical Research Coordinator (CRC) is an active participant in the coordination of oncology clinical trials from research planning and throughout the c Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Clinician, Healthcare


  • New York, United States Northwell Health Full time

    Coordinates and monitors research trials; actively oversees the recruitment of study participants. May be required to perform venipuncture on study participants; collects, processes, and ships specimens according to protocol and training requirements Research Coordinator, Clinical Research, Clinical, Coordinator, Research, Healthcare


  • New York, United States Icahn School of Medicine at Mount Sinai Full time

    A Clinical Research Coordinator (CRC) position is currently available within the Medicine Clinical Trials Office. Duties will include activities such as data collection and management of patient clinical information, timely collection of protocol related samples including shipment to outside entities as required, obtain informed consent, collect, maintain...


  • New York, United States Icahn School of Medicine at Mount Sinai Full time

    A Clinical Research Coordinator (CRC) position is currently available within the Medicine Clinical Trials Office. Duties will include activities such as data collection and management of patient clinical information, timely collection of protocol related samples including shipment to outside entities as required, obtain informed consent, collect, maintain...


  • New York, United States Medasource Full time

    Job Title: Clinical Research Coordinator II Location: New York City (Hybrid) Job Type: Full-time Duration: 6 month contract to hire PAY: $36-37 AN HOUR Overview: We are seeking a highly skilled Clinical Research Specialist to join our team in New York City. This role will involve working on lymphoma and leukemia clinical trials, contributing to the...