Oncology TMF Specialist (eTMF) – Quality & Compliance

A pharmaceutical company based in Baton Rouge is seeking a qualified candidate to manage Trial Master Files. The ideal candidate will have at least 3 years of clinical research experience, knowledge of eTMFs such as Veeva, and strong Microsoft Office skills. Responsibilities include ensuring the quality and maintenance of TMFs, conducting audits, and collaborating with various teams to guarantee compliance. Compensation ranges from $72,500 to $90,600, alongside a comprehensive benefits package and strong time-off policies. #J-18808-Ljbffr