Supervisor, Clinical Studies

Job DescriptionJob DescriptionStudy ManagerA Study Manager is responsible to ensure that quality research is conducted at 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. In addition, ensure study enrollment meets or exceed Sponsors'...

Job DescriptionJob DescriptionStudy ManagerA Study Manager is responsible to ensure that quality research is conducted at 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. In addition, ensure study enrollment meets or exceed Sponsors'...

Job DescriptionJob DescriptionStudy ManagerA Study Manager is responsible to ensure that quality research is conducted at 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. In addition, ensure study enrollment meets or exceed Sponsors'...

Job DescriptionJob DescriptionStudy Start Up Manager The Study Start Up Manager is responsible for overseeing all aspects of the study start life cycle within the Program Management Organization(PMO). This role provides direct leadership to all study start up staff and contracting staff.  This role will also provide a link to senior leadership through which...

MISSION STATEMENTThe mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research, and prevention, and through education for undergraduate and graduate students, trainees, and professionals, employees, and the public.SUMMARYThe...

MISSION STATEMENTThe mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research, and prevention, and through education for undergraduate and graduate students, trainees, and professionals, employees, and the public.SUMMARYThe...

Job DescriptionJob DescriptionProgram SupervisorThe Program Supervisor will oversee and manage the patient enrollment processes and the patient experience from the time of an appointment being scheduled through the time that the patient finishes their screening visit with the main focus on increasing conversions to randomization and decreasing on-site DNQs....

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

Senior Coordinator, Clinical Studies - Thoracic-Head & Neck Medical Oncology JOB SPECIFIC COMPETENCIESProtocol Management Independently performs protocol specific tasks including collection of sponsor questionnaires, feasibility of screening, collecting specimens, and submission of utilization requests.Works with the Nurse Managers to ensure consistency...

SUMMARY The Clinical Studies Coordinator collaborates with the research team and principal investigator to coordinate the institutional and federal approval procedures for research lab and clinical trials, budgets and budgeting processes, and contractual agreements as well as develop and maintain a thorough tracking system for all department protocols and...

The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating with staff regarding protocol information.Key FunctionsDesigns, implements, monitors, and reports on clinical research project status, ensuring on-time performance:...

Job Title: Sr. Clinical Studies Coordinator Duration: 6+ month contract, intent to hire Location: Onsite- Houston, TX The Senior Coordinator, Clinical Studies is responsible for the day-to-day management and oversight of protocol compliance, patient care, and coordination of clinical trials. This role includes collaborating with the principal investigator to...

Job Title: Sr. Clinical Studies Coordinator Duration: 6+ month contract, intent to hire Location: Onsite- Houston, TX The Senior Coordinator, Clinical Studies is responsible for the day-to-day management and oversight of protocol compliance, patient care, and coordination of clinical trials. This role includes collaborating with the principal investigator to...

The primary purpose of the Coordinator, Clinical Studies position is to collaborate with the research team and Principal Investigator (PI) to coordinate clinical trial subject accrual and data management activities for departmental clinical research, specifically for the Minimal Risk Team. Under the guidance of the Supervisor, Clinical Studies, the...

The primary purpose of the Coordinator, Clinical Studies position is to collaborate with the research team and Principal Investigator (PI) to coordinate clinical trial subject accrual and data management activities for departmental clinical research, specifically for the Minimal Risk Team. Under the guidance of the Supervisor, Clinical Studies, the...