Associate II, TMF Operations

📋 Description

• Process, review, classify, and resolve TMF documents across complex studies.
• Manage essential documents in electronic and hard-copy formats.
• Prepare TMF QC checklists and coordinate reviews with project teams.
• Conduct TMF quality control for regulatory compliance and ICH GCP.
• Work with eTMF systems to review, index, process, and maintain documentation.
• Apply standardized naming conventions to ensure complete, searchable records.

🎯 Requirements

• University degree preferred, Life Sciences or related discipline.
• Up to 1–2 years of TMF operations/records management experience.
• Understanding of clinical research principles and TMF purpose.
• Experience with data collection, indexing, and standardized naming conventions.
• Ability to work with electronic document repositories or eTMF platforms.
• Strong written and verbal communication, attention to detail.

🎁 Benefits

• Build TMF operations and clinical research experience in a global CRO.
• Exposure to international studies and project teams.
• Hands-on experience with electronic TMF/document management tech.
• Collaborate with professionals across clinical research teams.
• Supportive, inclusive environment with professional development.
• Equal opportunity and diversity commitment.