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The Start Up Lead is responsible for managing the site start-up strategy, overseeing execution and coordination of start-up activities, collaborating with stakeholders, and training less-experienced staff. They ensure timely delivery and quality of submissions, manage risks, and act as a Subject Matter Expert in site-specific start-up processes.
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.
The Senior Project Controls Engineer will lead project management efforts across various engineering domains by aligning with client departments, providing hands-on support, producing key project deliverables like budget estimates and project schedules, and proactively identifying challenges while contributing to the company’s mission.
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 Project Controls Engineer will oversee project controls deliverables such as budget estimates, detailed project schedules, and feasibility analyses while supporting cross-functional client departments and troubleshooting engineering challenges throughout manufacturing processes.
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 Senior Manager of Site Contract Management will oversee the Site Contracts team, ensuring timely contract delivery and alignment with study timelines. Responsibilities include managing a team, reviewing and negotiating contracts, establishing procedures, tracking contract metrics, and participating in strategic initiatives. The role includes collaboration with various stakeholders and representing the organization in meetings.
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.
The Senior Project Billing Analyst supports the Finance team with project billing responsibilities including financial reconciliation, project budgeting, invoicing, and revenue assurance. The role involves managing customer contracts, ensuring billing accuracy, and collaborating with various teams to resolve issues and improve processes.
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