Associate II, TMF Operations

📋 Description

• Support TMF records processing, review, maintenance, and archiving in global CRO setting.
• Perform TMF QC reviewer activities per SOPs and practices.
• Process and resolve rejected TMF documents across studies and sponsors.
• Manage essential documents in electronic and hard-copy formats.
• Prepare TMF quality control checklists and coordinate reviews.
• Collaborate with project teams across geographies on documentation issues.

🎯 Requirements

• University degree preferred, Life Sciences or related.
• Up to 1–2 years TMF ops, records management, or related.
• Basic understanding of clinical research principles and TMF purpose.
• Experience with data collection, indexing, naming conventions.
• Experience with electronic document repositories or eTMF systems.
• Strong written/verbal communication; attention to detail.

🎁 Benefits

• Exposure to TMF ops in global CRO environment.
• Work with international studies and sponsor portfolios.
• Hands-on with electronic TMF and document tech.
• Collaborative environment with professionals in clinical research.
• Supportive, inclusive culture and professional development.
• Meaningful work improving data integrity and patient outcomes.