Associate II, TMF Operations

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for an Associate II, TMF Operations based in Brazil.

We are seeking a detail-oriented Associate II, TMF Operations professional to support the quality, accuracy, and compliance of essential clinical trial documentation. In this remote role, you will review, process, and quality-check Trial Master File (TMF) documents across clinical studies and sponsor portfolios, helping ensure that records meet regulatory requirements and established quality standards. You will work with electronic Trial Master File (eTMF) systems and document management platforms to maintain complete, accurate, and well-organized clinical records. Collaborating with global project teams and records management colleagues, you will identify documentation issues, resolve rejected files, and support continuous quality improvement. Your work will contribute to the integrity of clinical research and help ensure that trial documentation remains inspection-ready throughout the document lifecycle. This opportunity is well suited to an organized professional who values accuracy, teamwork, and compliance in a regulated environment.