Associate II, TMF Operations

📋 Description

• Perform TMF Approver and/or TMF QC Reviewer activities per SOPs.
• Process, review, classify, and resolve TMF documents across studies.
• Manage electronic and hard-copy essential documents with accuracy.
• Prepare TMF quality control checklists and coordinate reviews.
• Conduct TMF quality control to ensure regulatory compliance.
• Work with electronic repositories and eTMF systems for indexing.

🎯 Requirements

• University degree preferred in Life Sciences or related field.
• Up to 1–2 years in TMF ops, records management, or CRO/pharma.
• Understanding of clinical research principles and TMF purpose.
• Experience with data collection, indexing, and naming conventions.
• Ability to work with electronic document systems and improve technical proficiency.
• Strong communication, attention to detail, and organizational skills.

🎁 Benefits

• Build TMF operations and clinical research experience in a global CRO.
• Exposure to international studies, sponsor portfolios, and best practices.
• Hands-on experience with electronic TMF and document management tech.
• Collaborate with experienced professionals across clinical teams.
• Supportive environment valuing collaboration, creativity, and development.
• Career development opportunities within a global organization.