Remote TMF Specialist for Clinical Trials

Sarah Cannon Research Institute; Tennessee; On-site; USD 60,000 - 80,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Clinical Project Associate to ensure the Trial Master File (TMF) is set up and maintained in audit-ready condition. You will collect and review essential documentation throughout studies, collaborate with investigators and staff, and support regulatory compliance and trial milestones.

This remote-based role within the United States emphasizes documentation quality, cross-functional teamwork, and proactive problem solving to drive successful

Qualifications

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

Responsibilities

• Set up and document upload of files to the TMF/eTMF.
• Perform initial quality review of documents prior to filing.
• Maintain the TMF in audit-ready condition from study start to completion.
• Assist with confirming qualifications of investigators and sites.
• Distribute and collect documents across sites; liaise with CRAs.
• Review study documents to ensure current, complete and accurate files.
• Other duties as assigned.

Skills

TMF management

Document review

Regulatory compliance

Cross-functional teamwork

Education

High School Diploma

Tools

TMF/eTMF systems

Trial management software

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Clinical Project Associate to ensure the Trial Master File (TMF) is set up and maintained in audit-ready condition. You will collect and review essential documentation throughout studies, collaborate with investigators and staff, and support regulatory compliance and trial milestones.

This remote-based role within the United States emphasizes documentation quality, cross-functional teamwork, and proactive problem solving to drive successful