Remote Clinical Trial Associate – TMF and Documentation (Oncology)

McKesson; Tennessee; Hybrid; USD 65,000 - 90,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Clinical Project Associate. The role ensures the Trial Master File (TMF) is set up and maintained in audit-ready condition, with review of documents throughout the study lifecycle and collaboration with cross-functional teams.

Responsibilities include TMF setup, quality review, and site qualification assistance. Remote-based in the US; relocation assistance and visa sponsorship are not available.

Qualifications

• Minimum High School Diploma or GED.
• At least 1 year of clinical research experience required; at least 3 years preferred.
• Oncology clinical research experience preferred.

Responsibilities

• Set up and maintain the TMF/eTMF files.
• Perform initial quality review of documents prior to upload.
• Collaborate with document specialists to keep TMF audit-ready from start to finish.
• Assist with confirming the qualifications of investigators and investigative sites.
• Distribute and collect study documents with sites throughout the trial lifecycle.
• Review study documents to ensure current, complete, and accurate records.

Skills

Documentation management

Cross-functional teamwork

Quality review

Education

High School Diploma or GED

Tools

TMF/eTMF systems

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Clinical Project Associate. The role ensures the Trial Master File (TMF) is set up and maintained in audit-ready condition, with review of documents throughout the study lifecycle and collaboration with cross-functional teams.

Responsibilities include TMF setup, quality review, and site qualification assistance. Remote-based in the US; relocation assistance and visa sponsorship are not available.