Senior Clinical Trials Coordinator, Thoracic Oncology

UT MD Anderson; Houston (TX); Presencial; USD 67.000 - 100.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health benefits

Paid time off

Tuition assistance

Pension plan

Descripción de la vacante

The University of Texas MD Anderson Cancer Center in Houston seeks a Senior Coordinator, Clinical Studies to coordinate and manage clinical research protocols from activation to completion. You will support Principal Investigators, oversee protocol operations, ensure regulatory compliance, and drive successful execution of study activities.

This role offers exposure to clinical trial operations, protocol management, research leadership, and cross‑functional coordination.

Formación

• Required: Bachelor’s Degree
• Preferred: Master’s Degree Public Health or related scientific field.

Responsabilidades

• Perform protocol-specific tasks, including screening participants, ordering tests, collecting specimens, and documenting patient-reported responses under supervision.
• Coordinate and attend assigned study meetings and individual meetings with the Principal Investigator.
• Provide all study-related coordination necessary for multi-site grants and research initiatives.
• Support protocol implementation and ongoing study activities to ensure project objectives are met.
• Oversee the effective operation of designated clinical research protocols.
• Collaborate with Principal Investigators and study sponsors to address operational and budget-related issues.
• Coordinate study deliverables, personnel issues, financial reconciliations, and budget projections.
• Develop, recommend, and implement clinical study revisions for Principal Investigator approval.
• Ensure protocol activities are completed in accordance with study requirements and timelines.
• Assist in the collection and evaluation of data for abstracts, research reports, funding proposals, operational documents, and procedure manuals.
• Support the preparation and maintenance of research documentation and study-related materials.
• Coordinate submission and maintenance of protocols associated with multi-site grant activities.
• Monitor study progress and support achievement of established objectives.
• Conduct periodic internal audits to ensure research activities comply with IRB-approved protocols.
• Review study operations to ensure compliance with grant specifications and protocol requirements.
• Identify and address operational issues that may impact study performance and compliance.
• Support continuous improvement of study processes and research operations.
• Train personnel responsible for specific functions or phases of assigned clinical research studies.
• Provide guidance and support to study staff involved in protocol activities.
• Assist with onboarding and education related to protocol-specific responsibilities.
• Perform other duties as assigned.

Educación

Bachelor's Degree

Master's Degree Public Health or related scientific field

Descripción del empleo

The University of Texas MD Anderson Cancer Center in Houston seeks a Senior Coordinator, Clinical Studies to coordinate and manage clinical research protocols from activation to completion. You will support Principal Investigators, oversee protocol operations, ensure regulatory compliance, and drive successful execution of study activities.

This role offers exposure to clinical trial operations, protocol management, research leadership, and cross‑functional coordination.