Remote Clinical Project Associate – TMF & Compliance

Sarah Cannon Research Institute; Nashville (TN); A distancia; USD 60.000 - 80.000; Jornada completa

Descripción de la vacante

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Project Associate to ensure the Trial Master File is audit-ready and to manage critical documentation across the study lifecycle. You will support cross-functional teams and use TMF/eTMF systems and related tracking tools.

This role is remote based in the US, and relocation assistance or visa sponsorship are not available.

Formación

• Minimum high school diploma or GED required.
• At least 1 year of clinical research experience required; 3+ years preferred.
• Oncology clinical research experience preferred.

Responsabilidades

• Set up and maintain the TMF/eTMF in audit-ready condition.
• Conduct initial quality review of documents prior to upload.
• Maintain TMF in audit-ready condition from study start to completion.
• Assist with confirming qualifications of investigators and sites.
• Distribute and collect study documents with investigative sites; liaise with CRA.
• Review study documents for currency, completeness, and accuracy.
• Perform other duties as assigned.

Conocimientos

Clinical research experience

Oncology experience

Educación

High School Diploma or GED

Descripción del empleo

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Project Associate to ensure the Trial Master File is audit-ready and to manage critical documentation across the study lifecycle. You will support cross-functional teams and use TMF/eTMF systems and related tracking tools.

This role is remote based in the US, and relocation assistance or visa sponsorship are not available.