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The Principal Quality Assurance Auditor oversees quality and compliance activities during clinical studies, serving as a subject matter expert. Responsibilities include supporting the Q&C team, conducting audits, coordinating vendor assessments, and providing training and guidance on quality systems while ensuring adherence to regulations.
The Commercial Strategy & Optimization Lead provides strategic guidance to enhance the effectiveness of the Commercial organization, collaborates with leaders across functions, and drives projects to improve commercial impact. Responsibilities include developing commercial strategy, improving sales opportunities, and managing multiple projects effectively.
The Safety Specialist II is responsible for processing and evaluating Serious Adverse Event reports, providing safety expertise, mentoring new staff, and interfacing with sponsors and vendors. The role supports the design and implementation of safety collection tools and reporting systems, with a strong focus on regulatory compliance and project-specific guidelines.
The Financial Analyst supports operational project teams with financial aspects during clinical trials, including invoicing, variance analysis, budget reviews, and financial reporting. The role involves collaboration with the finance team and providing assistance in contract preparation and internal controls development.
The Principal SAS Programmer is responsible for programming metrics, reports, and tools to support clinical trial data management from start to post database lock. This role also involves developing and validating SAS programs, providing biostatistics and data management support, ensuring project delivery, and offering training and leadership within project teams.
The Project Controls Engineer will coordinate with various departments to support engineering life cycles, perform due diligence to ensure high-quality project deliverables, identify and solve roadblocks, and produce key project controls deliverables including budgets and project schedules while fostering client relationships.
The Senior Project Controls Engineer will align with cross-functional teams, provide support for engineering processes, perform due diligence for project deliverables, identify roadblocks, and produce project controls documents including budget estimates and schedules while embodying the company's patient-focused mission.
Work as a Senior Project Engineer at Precision for Medicine, Manufacturing Solutions. Responsibilities include creating alignment with cross-functional client departments, providing hands-on support, authoring technical documents, and more. Requires a Bachelor's degree in Life Science, Engineering, or related discipline and at least 1 year of relevant experience.
The Document Control Specialist is responsible for managing controlled documents and records in adherence to quality assurance processes. Duties include facilitating document workflows, ensuring compliance with standards, conducting employee training, and preparing documents for audits.
As a CRA II, you will monitor and manage clinical studies, ensuring compliance with protocols and regulations. Responsibilities include coordinating site activities, preparing regulatory submissions, and identifying study risks. You will also travel domestically for site visits, contributing to oncology research.
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