Senior Clinical Trials Coordinator - Lead, Multi-Site & Compliance

UT MD Anderson Cancer Center; Texas; Presencial; USD 67.000 - 100.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical coverage starting day one

Paid time off

Tuition assistance

Pension plan

Descripción de la vacante

UT MD Anderson Cancer Center in Houston, TX seeks a Senior Coordinator, Clinical Studies to manage protocols from activation to completion, support Principal Investigators and sponsors, and lead study coordination across sites.

The role emphasizes regulatory compliance, quality oversight, staff training, and efficient study operations, with exposure to budgeting, data management, and multi-site grant activities.

Formación

• Bachelor’s Degree required.
• Preferred: Master’s Degree in Public Health or related field.
• Five years experience in research study or direct patient care (nursing, data gathering, or related).
• Experience with clinical trial management, budget oversight, staff training, and research compliance is highly valued.

Responsabilidades

• Perform protocol-specific tasks including screening, tests, specimens, and documenting responses under supervision.
• Coordinate and attend study meetings with the Principal Investigator.
• Provide study-related coordination for multi-site grants and research initiatives.
• Support protocol implementation and ongoing study activities to meet objectives.
• Oversee operation of designated clinical research protocols and budgets.
• Develop and implement study revisions for PI approval and ensure timelines are met.
• Assist in data collection for abstracts, reports, proposals, and manuals.
• Monitor study progress and ensure compliance with IRB-approved protocols.
• Train staff and assist with onboarding related to protocol responsibilities.

Educación

Bachelor’s Degree

Master’s Degree Public Health or related scientific field

Descripción del empleo

UT MD Anderson Cancer Center in Houston, TX seeks a Senior Coordinator, Clinical Studies to manage protocols from activation to completion, support Principal Investigators and sponsors, and lead study coordination across sites.

The role emphasizes regulatory compliance, quality oversight, staff training, and efficient study operations, with exposure to budgeting, data management, and multi-site grant activities.