Clinical Research Coordinator I, II

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...

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...

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,...

This is an entry-level coordinator position for the Precision Health Study (PHS). PHS is a meal-challenge study, with a focus on the dietary glycemic index of carbohydrates. The study lasts around 10 days, including a 7-day usual diet & lifestyle tracking period and a 3-day meal-challenging period. Participants will be recruited in the New Orleans...

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...

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,...

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...

This is an entry-level coordinator position for the Precision Health Study (PHS). PHS is a meal-challenge study, with a focus on the dietary glycemic index of carbohydrates. The study lasts around 10 days, including a 7-day usual diet & lifestyle tra Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Education

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

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

Research NursePediatrics - Hematology/OncologyLocation: New Orleans, LASummaryThis is a nursing research position. Training will be provided to develop the necessary skills required of a research nurse. The primary responsibility of the Research Nurse is to manage RN responsibilities in the conduct of clinical trials. This position also requires management...

The Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials supported by the Yale Cancer Center Clinical Trials Office (CTO). Key responsibilities include overseeing, plann Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Operations, Healthcare

The Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials within Yale Cancer Center Clinical Trials Office (CTO). Key responsibilities include overseeing, planning, track Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Operations, Healthcare

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...

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...

This is a nursing research position. Training will be provided to develop the necessary skills required of a research nurse. The primary responsibility of the Research Nurse is to manage RN responsibilities in the conduct of clinical trials. This position also requires management of global oncology research within the Hematology/Oncology department. The...

The Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials within Yale Cancer Center Clinical Trials Office (CTO). Key responsibilities include overseeing, planning, track Clinical Research, Research Coordinator, Clinical, Coordinator, Float, Research, Healthcare

Essential Duties 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, completion, and administration. 3. Contributes to study feasibility reviews and makes...

Essential Duties 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, completion, and administration. 3. Contributes to study feasibility reviews and makes...

Essential Duties 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, completion, and administration. 3. Contributes to study feasibility reviews and makes...