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The Principal Statistical Programmer leads programming activities for clinical studies, ensuring timely and high-quality deliverables. Responsibilities include supporting regulatory submissions, developing documentation, and collaborating with teams. Proficiency in SAS and knowledge of clinical development are essential.
The Principal Statistical Programmer leads programming efforts for clinical studies, ensuring timely and high-quality deliverables. Responsibilities include developing programming documentation, engaging with study teams, and supporting regulatory submissions.
As a Scientist at Regeneron, you will support the automation pipeline for CAR-T and TCR binder optimization. Responsibilities include designing CAR/TCR constructs, performing immunological assays, troubleshooting automated instruments, and maintaining tumor cell lines. A strong background in cell culture and experience with Hamilton liquid handlers are essential.
The Employee Listening Program Manager will manage the employee listening program, gather insights on employee sentiment, design and analyze surveys, and report findings to stakeholders. They will collaborate across departments, ensure data privacy, and continuously improve programs based on industry trends.
The Staff IT Operations Reporting Specialist is responsible for developing and managing reporting processes to enhance operational excellence in a regulated environment. Key duties include collaborating with stakeholders to gather reporting needs, designing innovative performance dashboards, analyzing data for trends, and ensuring compliance with regulatory standards.
The Senior Manager will lead a team of professionals in Global Procurement Compliance, focusing on cGMP compliance. Key responsibilities include managing supplier quality compliance, facilitating CAPAs, deviation investigations, and maintaining documentation. The role involves regular interfacing with Quality Assurance and overseeing the Approved Supplier List and supplier audit compliance. Continuous improvement initiatives and coaching team members are also essential duties.
The Senior QC Scientist will execute investigation testing for the identification of unknown materials, evaluate and interpret data, develop analytical methodologies, and supervise junior members. Responsibilities also include maintaining laboratory instruments, supporting regulatory inspections, and leading improvement initiatives while ensuring compliance with processes.
The Senior Reliability Engineer will lead reliability improvements, support mechanical reliability issues, conduct troubleshooting, analyze equipment failures, and develop engineering solutions to ensure equipment uptime. Additionally, they will maintain compliance with regulatory standards and implement reliability monitoring programs.
The Compliance Manager (Technical Operations) oversees cGMP compliance for Technical Operations, evaluates adherence to regulations, manages audit readiness, coordinates training and compliance efforts, and liaises with Quality Assurance. The role requires effective supervision and leadership, along with strong communication and problem-solving skills.
The Senior Statistical Programmer supports study teams by providing programming expertise essential for processing clinical trial data. Responsibilities include coding, designing program logic, overseeing projects for statistical analyses, and ensuring compliance with internal standards. The role involves managing data integration across studies, creating programming specifications, and supporting submissions for regulatory approvals.
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