Thermo Fisher Scientific
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As a Programmer Analyst - SAS, you will program and validate data transfers across systems, prepare clinical trial datasets, consult with researchers, and potentially lead projects while ensuring compliance with SOPs and contributing to departmental processes.
The Biostatistician leads statistical project responsibilities including developing analysis databases, conducting statistical analyses, and generating formatted summaries. This role includes ensuring compliance with departmental procedures, developing statistical analysis plans, providing mentorship, and managing project timelines and budgets.
As a Database Administrator III, you will design, develop, and implement scalable database services, ensuring efficient operation and collaboration with IT professionals. Your role will include creating reports and dashboards, automating database processes, and maintaining database environments to run issue-free.
The Clinical Trial Coordinator will support clinical study delivery, manage operational aspects, collaborate with partners, monitor study progress, and ensure adherence to timelines, budgets, and quality standards. Responsibilities include maintaining databases, tracking compliance, coordinating vendor management, and ensuring studies are inspection-ready with complete documentation.
The Trial Activation Approval Specialist I prepares submissions for clinical trial approvals, collects essential documents, reviews IP greenlight packages, and ensures timely site activations while maintaining compliance with regulatory standards. This role involves collaboration with various teams and meticulous documentation of all processes.
The Localization Engineer provides engineering and technical services for complex localization projects, ensuring high-quality translations and implementations. Responsibilities include managing localization tasks, converting various formats for translation, troubleshooting, and collaborating with project teams to deliver results under tight deadlines.
