Trabajos irb en Texas (TX) State

At Houston Methodist, the Research Coordinator position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. This position ensures accurate data collection, documentation, organization ...

At Houston Methodist, the Clinical Research Specialist position is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols, gathering patient data via methods specified in the study protocol, study reports. This positi...

JOB SUMMARY At Houston Methodist, the Director Respiratory Care Services position is responsible for 24-hour management of the Respiratory Care Department and Pulmonary Function Laboratory which includes short and long-term planning, program and staff development, resource and budget management, ...

At Houston Methodist, the Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. Under minimal supervision, this position is responsible for ensuring acc...

At Houston Methodist, the Research Coordinator position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. This position ensures accurate data collection, documentation, organization ...

At Houston Methodist, the Research Coordinator position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. This position ensures accurate data collection, documentation, organization ...

At Houston Methodist, the Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. Under minimal supervision, this position is responsible for ensuring accu...

With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. As the on...

At Houston Methodist, the Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. Under minimal supervision, this position is responsible for ensuring acc...

In partnership with the Organizational Official (OO), the Director, IRB Operations & Compliance Director, IRB Operations & Compliance plans, directs, and oversees the IRB operations including policies, objectives, and initiatives to ensure company compliance with federal regulations, ICH/GCP (E6)...

This position performs quality assessments of primarily minimal risk submissions and deliverables to ensure completeness, accuracy, and compliance with applicable regulations and standard operating procedures. ...

Position Overview: In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent process and monitor patient status and safety; collect and organize research data; schedule and conduct study-specific training and site in-services to study related s...

Assists Regulatory to create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements. * Reviews new protocols and other ...

Sponsor-provided and IRB-approved Protocol Training * All relevant Protocol Amendments Training * Any study-specific Manuals Training, as applicable * Sponsor-specified EDC and/or IVRS and any other ...

Institutional Review Board Coordinator / IRB Shift: Full time - Days *Onsite* Location: Medical City Plano Hospital Introduction Are you looking for a work environment where diversity and inclusion ...

Ethics Committee and IRB Interaction: Communicate with ethics committees or IRBs to address queries, provide updates, and secure timely approvals. * Site Support: Provide continuous support to ...

... IRB. • Documents all regulatory research and administrative actions to ensure study compliance. • Prepares/delivers required reports and other research documentation to PI. • Prepares ...

... IRB-approved protocols. Project Management: • Develop and maintain study timelines and ensure milestones are met. • Coordinate study meetings and communicate updates to the research team

Report Adverse and Serious Adverse Events to IRB and Sponsor following guidelines. * Obtain and document informed consent following ICH/GCP and site SOPs. * Ensure timely and accurate data entry ...

Support clinical operations activities including IRB/ethics submissions, data collection, discrepancy resolutions, monitoring activities, data analysis/reporting plans, safety oversight workflows ...

Sponsor-provided and IRB-approved Protocol Training * b. All relevant Protocol Amendments Training * c. Any study-specific Manuals Training, as applicable * d. Sponsor-specified EDC and/or IVRS and ...

In general, the CRC ensures the clinical study maintains accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements

Perform technical tax research and analysis for special initiatives such as property tax and IRB. * Coordinate the preparation of Federal, State, and withholding tax returns on a monthly, quarterly ...

Ensures IRB approved protocols are implemented and followed. Executes informed consent process and monitors patient status and safety; collects and organizes research data; schedules and conducts ...