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The Senior Manager of Contracting will lead a new team in Global Procurement at Regeneron, overseeing contract management and establishing efficient workflows. This role involves collaboration with partners to negotiate agreements, implementing best practices in contracting, and mentoring team members to ensure compliance with procurement policies in the biopharmaceutical industry.
The Principal Statistical Programmer will lead programming activities for clinical studies, ensuring timely and high-quality deliverables. Responsibilities include programming documentation, regulatory submission support, and collaboration with internal and external teams. Required skills include proficiency in SAS and knowledge of statistical concepts and clinical trial principles.
As a QA Specialist, you will ensure manufacturing documentation aligns with quality standards, participate in investigations and problem resolution, train junior employees, review controlled documents, and represent QA in cross-functional meetings. You'll focus on continuous evaluation of procedures and support technical transfer activities through documentation oversight.
As a Data Loss Protection Engineer, you will contribute to developing a DLP strategy, evaluate and design secure DLP solutions, and ensure compliance with regulatory requirements. Your role will involve providing support for DLP related incidents, optimizing DLP tools, and collaborating with various teams to enhance data security across the organization.
The Senior Analyst for Performance and Analytics will manage analytics and reporting for the Global Procurement team. Responsibilities include creating performance metrics, supporting e-sourcing events, managing project timelines, and collaborating with cross-functional teams to improve processes. The role requires strong analytical and interpersonal skills.
The Senior Specialist in Category Management at Regeneron will support the global procurement team's strategy development, assist in the sourcing processes, manage and analyze supplier responses, archive category materials, and contribute to continuous improvement efforts. This role focuses on leveraging extensive experience in procurement within the Pharma/BioPharma domain.
The Senior Statistical Programmer supports study teams by implementing programming standards and maintaining documentation for clinical studies. This role includes providing programming deliverables for study reports, regulatory submissions, and ad hoc analyses while collaborating with cross-functional teams to ensure compliance and traceability in accordance with regulations.
The Senior Staff Supply Compliance Analyst leads compliance activities in Supply Chain Management, develops compliance frameworks, acts as a liaison between departments, facilitates policy reviews, and manages compliance investigations while ensuring timely documentation and corrective actions are implemented effectively.
The Administrative Coordinator provides administrative and project support to the Corporate Affairs department, including budget tracking, Purchase Order management, scheduling for the SVP, and event coordination. Key responsibilities also involve vendor onboarding, meeting logistics, and supporting team communication and inquiries.
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.
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