Regeneron

Compliance

• Manage and identify opportunities to improve core privacy operations, including Privacy Impact Assessment, Record of Processing Activities, and Data Subject Access Request processes
• Lead complex privacy program initiatives across business functions
• Leverage technology and AI to automate and improve privacy operations
• Document advice and implementation of online privacy notices, controls, tracking technologies, and privacy-enhancing tools
• Develop and maintain privacy program metrics and KPIs
• Maintain internal policies, procedures, guidance documents, training and awareness, and the Intranet site
• Coordinate Privacy Steward engagement for enterprise-wide privacy initiatives
• Manage vendor relationships, Statements of Work, requisitions, purchase orders, and invoices

Senior Manager, Data Privacy Operations

General

• Support in vitro safety and efficacy testing of cell therapy candidates
• Develop tumor antigen expression and flow cytometry methods
• Contribute to viral-vector production and process development for cell engineering
• Support high-throughput protein production activities
• Contribute to analytical method development supporting Good Manufacturing Practice (GMP) manufacturing
• Support digital-transformation initiatives for manufacturing operations
• Document experimental procedures and results
• Collaborate with scientists across the cell therapy team

Co-op, Cell Medicines Research & Development

• Develop and run LC-MS and MSI methods to characterize therapeutic proteins, bioconjugates, and biomarkers
• Apply CID and ExD mass spectrometry fragmentation techniques to characterize conjugated payloads
• Use CE-MS and iCIEF to characterize protein charge variants
• Build reference databases and spectral libraries
• Process and interpret mass spectrometry data to validate molecular structures
• Run high-throughput proteomics workflows using DIA methods and perform database searching with FDR control
• Develop and evaluate platform immunoassays, including ELISA and western blot methods
• Support development and purification of ADCs using conjugation chemistries, chromatography, and peptide mapping techniques
• Compare platform performance across bioconjugate modalities
• Document experimental procedures and results
• Present findings to the broader analytical sciences team

Co-op Analytical & Bioanalytical Sciences

Supply Chain

• Build planning, forecasting, and inventory-management tools and dashboards for clinical trial and supply chain operations
• Develop interactive web applications and resource maps to improve supply-chain visibility and efficiency
• Support day-to-day clinical supply operations
• Research and evaluate suppliers, materials, and sourcing opportunities
• Support supplier relationship management, category strategy development, and spend analytics
• Analyze data and apply digital tools, including AI and automation platforms
• Document processes and maintain organized records
• Contribute to continuous-improvement initiatives
• Collaborate with cross-functional teams and present findings and recommendations

Co-op, Supply Chain and Clinical Drug Logistics

Manager

• Lead country-cluster operations and field-based Clinical Trial Liaison teams
• Lead Clinical Trial Liaison performance, development planning, formal reviews, goals, workload, and quality delivery
• Oversee vendor-provided staff against service-level agreements and raise performance concerns
• Implement standardised feasibility, site selection, recruitment, retention, and investigator issue-resolution processes
• Advise cross-functional forums on study, programme, country, capacity, and resource strategies
• Build investigator relationships
• Conduct remote and on-site co-visits
• Support meetings, audits, and inspections
• Report monthly metrics, standard methodologies, issues, and escalations
• Retain a 15% liaison workload
• Foster a collaborative, high-performing cluster aligned with regional standards and continuous improvement
• Collaborate with regional leaders, study teams, vendors, and investigator sites

Senior Manager, Country Cluster Manager

Co-op Cell Medicines Research and Development

• Build planning, forecasting, and inventory-management tools and dashboards for clinical trial and supply chain operations
• Develop interactive web applications and resource maps to improve supply chain visibility and efficiency
• Support day-to-day clinical supply operations
• Research and evaluate suppliers, materials, and sourcing opportunities
• Support supplier relationship management, category strategy development, and spend analytics
• Analyze data and use artificial intelligence and automation platforms to streamline supply chain processes and decision-making
• Document processes and maintain organized records
• Contribute to continuous-improvement initiatives
• Collaborate with cross-functional teams and present findings and recommendations

Co-op Supply Chain, Clinical Drug Logistics

• Develop and run LC-MS and MSI methods to characterize therapeutic proteins, bioconjugates, and biomarkers
• Apply CID and ExD mass spectrometry fragmentation techniques to characterize conjugated payloads
• Use CE-MS and iCIEF to characterize protein charge variants
• Build reference databases and spectral libraries
• Process and interpret mass spectrometry data to validate molecular structures
• Run high-throughput proteomics workflows using DIA methods and perform database searching with FDR control
• Develop and evaluate platform immunoassays, including ELISA and western blot methods
• Support development and purification of antibody-drug conjugates using conjugation chemistries, chromatography, and peptide mapping
• Compare platform performance across different bioconjugate modalities
• Document experimental procedures and results
• Present findings to the broader analytical sciences team

Director

• Oversee country- and/or regional-level pharmacovigilance execution within the assigned region
• Ensure local safety activities follow global standards and local regulatory requirements
• Ensure country-generated safety data are accurately and timely integrated into the global PV system
• Serve as the escalation point for local execution issues and conduit between local operations and global oversight functions
• Maintain understanding of local legislation and Health Authority requirements
• Inform WWOO leadership of local requirement or process updates
• Track local process status, changes, and risks using common tools such as trackers or dashboards
• Develop innovative approaches incorporating new technologies, including AI
• Ensure country compliance with the global PV quality system
• Support inspections, audits, CAPAs, and resolution of deviations or non-compliance
• Coordinate with global GPS, non-GPS, and other PV hub teams
• Guide global teams on local requirements and compliance
• Shape compliant programs that provide high-quality adverse event reports
• Build, coach, and scale a high-performing team
• Drive succession planning and talent pipelines

Director, Pharmacovigilance Hub – Americas

• Lead and develop the national Allergy Thought Leader Liaison team, including performance management, coaching, succession planning, and career development
• Build a high-performing and inclusive team culture grounded in accountability, collaboration, sound judgment, and company values
• Set the national Allergy TLL strategy and translate brand priorities into field plans and execution
• Oversee thought-leader engagement, congress and conference presence, speaker-training strategy and execution, and speaker program execution
• Bring field and customer insights into brand planning
• Partner with marketing, field, medical, market access, and other teams to develop and refine business plans
• Build alliance partnerships and align priorities, roles, operating processes, and execution across organizations
• Manage the TLL budget and operating model, including resource allocation, team processes, vendor support, and performance measurement
• Maintain compliance and sound judgment across thought-leader engagement, congress activity, speaker programs, operating practices, and travel and expense management
• Report to the Senior Director, CRSwNP/AFRS Marketing

Director, Thought Leader Liaison – Allergy/ENT

Medical Director

• Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas
• Work independently and as part of integrated discovery and development teams
• Interpret pharmacologic and toxicity-related findings to advance promising therapeutics through Regeneron’s pipeline
• Determine and evaluate clinical pathology-related endpoints in pharmacology and toxicology studies
• Guide decision-making based on clinical pathology findings
• Collaborate with anatomic pathologists, toxicologists, and researchers within Regeneron
• Partner with CROs to provide scientific peer review of nonclinical safety studies
• Manage Clinical Pathology support for selected therapeutic focus areas
• Mentor junior Pathologists
• Support drug molecule efficacy and safety studies, including GLP toxicology and PK studies

Associate Director, Clinical Pathologist

Content Writer

• Coordinate authors of regulatory documents from a variety of disciplines within assigned projects
• Monitor project timelines and resources, escalating risks to management and supporting timeline negotiations across functional areas
• Identify training and development needs of direct reports, providing support and guidance for personnel
• Participate in screening and interviewing candidates to satisfy existing and new team needs
• Support the creation and maintenance of document templates, SOPs, and working practices
• Monitor adherence to document processes, escalating deviations to SW management
• Identify areas for process improvement within assigned projects and communicate observations to management
• Participate in relevant cross-functional drug development team meetings
• Support assignment of deliverables and definition of project priorities under the direction of senior Scientific Writing team members
• Coordinate regulatory document authors across disciplines, monitor document quality, and support staff training and professional development

Associate Manager, Scientific Writing

Clinical Research

• Provide oversight of lead Data Managers on assigned clinical data management studies
• Serve as DM study lead and primary point of contact for clinical study teams, external data vendors, and CROs
• Oversee data management activities from study start-up through archiving
• Provide data management expertise and hands-on support related to eCRF and database design, data quality, and reporting
• Oversee data quality review and data acceptance procedures before data analyses and/or database lock
• Manage data transfers, SAE/AE reconciliation, and MedDRA/WHO-DD coding
• Support study database transfer, locking, and archiving
• Manage scheduling and time constraints across multiple projects
• Prepare recommendations for improved data management processes and data flow
• Oversee CRO data management activities and ensure eCRF, clinical trial database, and electronic edit check execution follows SOPs and WIs
• Identify data quality, CRO performance, documentation, and process execution gaps and ensure resolution
• Document sponsor oversight from protocol review through study close-out
• Review and approve study documentation
• Perform quality review and inspection readiness tasks for quarterly IRR compliance
• Lead and oversee data management deliverables, timelines, snapshot/lock plans, status metrics, and program-level inputs
• Monitor data quality and data issue remediation
• Identify risks, propose mitigations, and proactively escalate operational, vendor, or CRO issues
• Provide limited program-level support for small programs

Manager, Clinical Data Management Study Lead

Clinical Specialist

• Provide technical and administrative support to clinical study teams executing trials across a program
• Help ensure studies stay on track from site activation through close-out
• Organize and deliver analyzable reports and metrics
• Coordinate study team meetings, agendas, and minutes
• Collate data for feasibility and site selection assessments
• Contribute to review of study documents and reference materials
• Track site activation, enrollment, and monitoring visits against projected plans
• Escalate issues or delays and monitor investigator/site status and registry postings
• Ensure timely receipt of scheduled reports and perform TMF reconciliations with study lead guidance
• Communicate with sites and maintain site contact information and internal and external relationships
• Contribute to close-out activities and support oversight of third-party vendors
• Investigate the impact of new information on trials
• Participate in SOP revisions and departmental initiatives
• Recommend process improvements

Clinical Study Specialist

Business Analyst

• Plan, coordinate, and deliver commercial operations projects
• Manage timelines, milestones, risks, and dependencies
• Lead project governance, including status reporting, RAID management, action tracking, meeting facilitation, and stakeholder communications
• Gather, analyze, and document business requirements
• Translate operational needs into functional requirements, user stories, and process improvements
• Support Veeva CRM and Veeva Events activities, including improvements, user support, data quality management, reporting, and system optimization
• Contribute to CRM transformation through current-state assessments, user acceptance testing, training coordination, and deployment support
• Coordinate meetings, events, and business planning activities
• Partner with Commercial Operations, Sales, Marketing, IT, and in-country teams to improve processes and operational efficiency

Senior Manager, Data Privacy Operations

Co-op, Cell Medicines Research & Development

Co-op Analytical & Bioanalytical Sciences

Co-op, Supply Chain and Clinical Drug Logistics

Senior Manager, Country Cluster Manager

Co-op Cell Medicines Research and Development

Co-op Supply Chain, Clinical Drug Logistics

Co-op Analytical & Bioanalytical Sciences

Director, Pharmacovigilance Hub – Americas

Director, Thought Leader Liaison – Allergy/ENT

Associate Director, Clinical Pathologist

Associate Manager, Scientific Writing

Manager, Clinical Data Management Study Lead

Clinical Study Specialist

Senior Business Analyst – Commercial Systems and Operations