Remote Clinical Project Associate — TMF & Trials

McKesson; Alaska; Remote; USD 70,000 - 90,000; Full time

Benefits offered by this job

Total Rewards package

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Project Associate for remote work in the United States. You will set up the TMF/eTMF, conduct quality reviews, and ensure audit-ready documentation throughout the trial lifecycle.

You will support investigator qualifications, coordinate with sites and CRAs, and help maintain regulatory compliance while contributing to cross-functional teams. Relocation or visa sponsorship are not offered.

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 document collection/upload of files to the TMF/eTMF.
• Perform initial quality review of documents prior to upload/filing in TMF/eTMF.
• Partner with document specialist to maintain the TMF in audit-ready condition from start to completion.
• Assist with confirming qualifications of investigators and investigative sites.
• Liaise with Clinical Research Associate and sites to resolve regulatory issues.
• Review study documents to ensure they are current, complete and accurate.
• Perform other duties as assigned.

Skills

TMF management

Documentation review

Cross-functional collaboration

Attention to detail

Education

High School Diploma or GED

Tools

eTMF software

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Project Associate for remote work in the United States. You will set up the TMF/eTMF, conduct quality reviews, and ensure audit-ready documentation throughout the trial lifecycle.

You will support investigator qualifications, coordinate with sites and CRAs, and help maintain regulatory compliance while contributing to cross-functional teams. Relocation or visa sponsorship are not offered.