Description
Allucent is hiring a TMF Lead to coordinate and oversee the creation, maintenance, completeness, quality, and timeliness of trial master files for assigned clinical studies. The role manages TMF specialists and cross-functional stakeholders, supports audits and inspections, monitors budgets, provides training, and contributes to process improvement and client-facing activities. Candidates need a life science, healthcare, or business degree, at least five years of TMF filing and quality-management experience, and at least five years of drug development or clinical research experience. The position is remote or hybrid depending on location, with two office days per week for employees within reasonable distance of a global office.
