- Knowledge of good clinical research practice.
- In-depth knowledge of IRB submission process and requirements.
- Ability to interact well with staff, participants, 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], advanced word processing [e.g., Word], and statistical analysis [e.g., SAS or Stata]).
- Ability to acquire and maintain all required CITI training certificates.
- Ability to acquire and maintain credentialing at all required institutions: Tulane Medical Center and partner institutions in Jamaica and Colombia.
- Bachelor's Degree or RN with five (5) years of related work experience.
- A Master's Degree in a related field with (2) years of related work experience.
- Master's Degree in Epidemiology, Clinical Research, or a related area.
- Experience in managing clinical or community research programs.
- Knowledge in computer software and database program.
- Ability to use Spanish as a working language.
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Clinical Research Coordinator
1 week ago
Tulane University New Orleans, United StatesThe 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 ...
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Clinical Research Coordinator
5 days ago
Tulane University New Orleans, United StatesCoordinates 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 C ...
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Clinical Research Coordinator
2 weeks ago
Tulane University New Orleans, United StatesCoordinates 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, Clinica ...
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Senior Clinical Research
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Tulane University New Orleans, United StatesThe primary responsibility of the Senior Clinical Research Coordinator is to manage and coordinate all aspects of conducting clinical trials and other epidemiological studies. The Senior Clinical Research Coordinator supervises clinical research staf Clinical Research, Research C ...
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Clinical Research Coordinator
2 weeks ago
Tulane University New Orleans, United StatesCoordinates 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 rese ...
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RN Clinical Research
5 days ago
Ochsner Health New Orleans, LA, United StatesWe've made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate. We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who f ...
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Clinical Research Coordinator
5 days ago
Tulane University New Orleans, United StatesCoordinates 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 ...
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Clinical Research Coordinator
5 days ago
Ochsner Health System New Orleans, United StatesWe've made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate. We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who f ...
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Clinical Research Nurse
5 days ago
Ochsner Health System New Orleans, LA, United StatesWe've made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate. We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who f ...
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Clinical Research Coordinator
2 weeks ago
Tulane University New Orleans, United States StaffSummary · 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 ...
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Clinical Research Coordinator
2 weeks ago
Tulane University New Orleans, United States StaffSummary · 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 On ...
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Clinical Research Coordinator
2 weeks ago
Tulane University New Orleans, United States StaffSummary · 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 p ...
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Clinical Research Coordinator
14 hours ago
Tulane University New Orleans, United StatesClinical Research Coordinator (I, II, and III)EpidemiologyLocation: New Orleans, LA · SummaryThe 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 ...
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Clinical Research Coordinator II
5 days ago
Tulane University New Orleans, United StatesThe 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 s ...
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Clinical Research Coordinator, CHERISH
5 days ago
Tulane University New Orleans, United StatesThe 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 C ...
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Clinical Research Coordinator I
5 days ago
Tulane University New Orleans, United StatesThe 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 C ...
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Clinical Research Coordinator I
5 days ago
Tulane University New Orleans, United StatesThe 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 ...
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Associate Clinical Research Coordinator
5 days ago
Ochsner Health New Orleans, United StatesWe've made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate. We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who f ...
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Clinical Research Coordinator I
5 days ago
Tulane University New Orleans, United StatesThe 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 ...
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Clinical Research Coordinator III
5 days ago
Tulane University New Orleans, United StatesThe 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, Resear ...
Senior Clinical Research - New Orleans, United States - Tulane University
Description
The primary responsibility of the Senior Clinical Research Coordinator is to manage the daily operations of the study data and coordinating center for a hypertension control project taking place in Jamaica and Colombia.
The Senior Clinical Research Coordinator is required to have an in-depth knowledge of clinical research protocol requirements and good clinical practices as set forth by federal regulations.
This position trains and supervises study staff to ensure compliance with study protocols and overall study objectives.
The Senior Clinical Research Coordinator acts as a liaison between the investigators in the United States, Colombia, and Jamaica, other collaborators, the Institutional Review Board, and government agencies.
The Senior Clinical Research Coordinator coordinates all research-related activities, including the initial set-up of the study, study participant recruitment and retention, delivery of the intervention, data collection, entry, and quality control activities, protocol compliance and patient safety.
This position works on monitoring data quality assurance and quality control and study conduct. This position works independently in designing, coordinating, and implementing all assignments.
The Senior Clinical Research Coordinator is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.
This position serves as a key management and administrative role for clinical research projects conducted in the department by supervising clinical research staff to ensure compliance with protocol, federal, and institutional requirements.
Some travel to study sites in Jamaica and Colombia will be required for training and site visits.
Ability to complete and pass successfully the required occupational health screening referenced in the University's Animal Handler Health Surveillance Program on an annual basis.
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.