Associate II, TMF Operations

📋 Description

• Support TMF records processing and review across complex studies.
• Manage essential documents in electronic and hard-copy formats.
• Prepare TMF quality control checklists and coordinate reviews.
• Conduct TMF quality checks for regulatory and SOP alignment.
• Work with eTMF systems to review, index, and maintain documentation.
• Apply standardized naming conventions and indexing for inspection-readiness.

🎯 Requirements

• University degree preferred, Life Sciences or related.
• 1–2 years in TMF ops, records mgmt, or clinical research.
• Understanding of clinical research principles and TMF purpose.
• Experience with data collection, indexing, and naming conventions.
• Experience with electronic repositories/eTMF; willingness to upskill.
• Strong written/verbal communication and attention to detail.

🎁 Benefits

• Hands-on TMF and clinical research exposure in a global CRO.
• International study exposure and collaboration with teams.
• Experience with electronic TMF and document management tools.
• Collaborative, inclusive work environment and professional development.
• Opportunities for career growth within a global org focused on patient outcomes.
• Commitment to equal opportunity and respectful collaboration.