The TMF Representative is responsible for the preparation, maintenance, and indexing of Trial Master Files to ensure compliance with study protocols and regulatory requirements. They will also act as a point of contact for sponsors, project managers, and study sites to facilitate effective communication and study documentation.
The Veeva Clinical Database Programmer will administer EDC trials, including eCRF design, edit check programming, and database configuration. They will also serve as a subject matter expert for the Veeva CDMS suite and ensure high-integrity data imports while maintaining global clinical trial standards.
Support the development of scopes, budgets, and pricing for bioanalytical studies while collaborating with cross-functional teams. Manage the financial lifecycle of awarded projects, including forecasting, invoice preparation, and project close-out activities.
Support the development of scopes, budgets, and pricing for bioanalytical studies while collaborating with cross-functional teams. Manage the financial lifecycle of awarded projects, including forecasting, invoice preparation, and project close-out activities.
