5 pharmacy manager jobs found

The Clinical Research Coordinator (CRC) will work within the adult Leukemia clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the...

The CRC (Clinical Research Coordinators) work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under the direction of the Supervisor of Research Oncology Informatics, the Research Oncology Informatics Pharmacist plays a critical role in supporting the successful implementation of investigational therapies within Epic. This position partners closely with Principal Investigators, Research Nurses, Research Assistants, and other Cancer Clinical Trials Office staff to design, build, and maintain investigational medication records in Willow and treatment plans in Beacon. The pharmacist provides oversight of adult research chemotherapy treatment plans, ensuring accuracy, regulatory compliance, and operational efficiency. Through close collaboration with Hematology/Oncology investigators and research teams, this role helps ensure timely review, approval, and ongoing management of investigational treatment plans, supporting high-quality clinical research and patient...

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under the direction of the Supervisor of Research Oncology Informatics, the Research Oncology Informatics Pharmacist plays a critical role in supporting the successful implementation of investigational therapies within Epic. This position partners closely with Principal Investigators, Research Nurses, Research Assistants, and other Cancer Clinical Trials Office staff to design, build, and maintain investigational medication records in Willow and treatment plans in Beacon. The pharmacist provides oversight of adult research chemotherapy treatment plans, ensuring accuracy, regulatory compliance, and operational efficiency. Through close collaboration with Hematology/Oncology investigators and research teams, this role helps ensure timely review, approval, and ongoing management of investigational treatment plans, supporting high-quality clinical research and patient...

The CRC (Clinical Research Coordinators) work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials...