Associate II, TMF Operations

📋 Description

• Support TMF processing, review, and QC in SOPs and working practices.
• Process and resolve rejected TMF documents across complex studies.
• Manage essential documents in electronic and hard-copy formats.
• Prepare TMF Quality Control checklists and coordinate reviews.
• Contribute to TMF compliance, regulatory expectations, and best practices.
• Collaborate with project teams across functions and geographies.

🎯 Requirements

• University degree preferred, Life Sciences or related
• Up to 1–2 years TMF ops, records mgmt, or clinical research experience
• Understanding of clinical research principles and TMF purpose
• Experience with data collection, indexing, naming conventions
• Experience with electronic document repositories or eTMF systems
• Strong communication, attention to detail, and organizational skills

🎁 Benefits

• Exposure to global CRO environment and TMF operations
• Experience with electronic TMF and document management technologies
• Collaboration with experienced professionals across clinical research
• Supportive, inclusive work environment and professional development
• Equal opportunity and diverse, respectful collaboration
• Opportunity to contribute to data integrity and patient outcomes