Trial Documentation Associate I

Key Responsibilities:

• Provide ongoing assistance to support clinical research operations, including study documentation maintenance and monitoring reports.
• Collect, review, and maintain essential documents, and activate new or amended protocols at an institutional level.
• Track and update documentation, study status, and key milestones within CTMS, eTMF, and other systems.

Qualifications:

• Bachelor's degree in a relevant area required.
• Prior experience with clinical research operations, TMF/eTMF setup, and ICH/GCP guidelines preferred.
• Strong proficiency in managing flow of clinical trial regulatory documents and study start-up activities.

Work Environment:

• This is a remote position within approved U.S. locations, excluding California.
• St. Jude is an Equal Opportunity Employer with a commitment to finding cures and saving children.