Regeneron

Manager

• accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out
• ensures study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP
• leads the cross-functional study team responsible for clinical study delivery
• oversees execution against planned timelines, deliverables, and budget while escalating issues to the Program Operations Lead
• provides operational input into protocol development
• oversees or conducts site evaluation and selection
• leads investigator meeting preparation and execution
• manages study close-out activities, including database lock, reconciliation of vendor contracts, and budget

Manager, Clinical Study Lead

Program Manager

• provide operational leadership and manage components of development programs
• contribute to the cross-functional development team to develop strategic plans including goals, budgets, timelines and track execution from preclinical through commercialization/lifecycle management
• support select subteam and/or functional area meetings under the direction of a manager or DPM Lead
• identify stakeholders across the organization to facilitate cross-functional reviews/alignments of key documents
• track deliverables, risks, and issues
• escalate issues/risks to appropriate stakeholders in a timely manner
• gather information relevant to issues and formulate solutions
• build relationships and effectively collaborate with department and cross-functional colleagues

Manager, Development Program Management

• Provide operational direction as the leader for one or more development programs
• Execute the strategic direction of a program from preclinical through commercialization
• Drive the development and implementation of integrated project program plans, goals, budgets, and timelines
• Form and manage effective cross-functional teams
• Support the development of a program throughout its lifecycle
• Assess and proactively address the needs of the program from pre-IND through commercialization
• Actively aim to strengthen and lead high performance teams
• Develop contingency and risk mitigation plans
• Manage project/program interactions and deliverables between Regeneron and strategic alliance partners

Senior Manager, Development Program Management

Operations

• Ensuring operational activities between Regeneron and external laboratory partners run efficiently
• Acting as core internal liaison between external lab partners and Regeneron colleagues
• Overseeing laboratory issues by providing oversight, solutions, and support
• Ensuring collaboration with Vendor Management, Quality Assurance, and other departments
• Triage, manage, and mitigate risk associated with external laboratory partner escalations
• Liaise with external lab partners to create and maintain training documents
• Identify and lead process improvements at external laboratory partners
• Support quality audits and scientific alignment with external laboratory partners
• Monitor and improve key stakeholder performance at external laboratory partners

Manager, Precision Medicine Operations – Lab Manager

Artificial Intelligence

• Implement, and refine novel algorithms and scalable AI /ML solutions tailored to GD applications such as clinical trial design, regulatory intelligence, patient identification and stratification, etc.
• Deploy these solutions to production environments as appropriate
• Implementation includes hands-on development and coding.
• Develop, implement, and improve data architecture and engineering approaches for diverse data sources across GD
• Contribute to initiatives with GDIT and enterprise IT to build the necessary infrastructure (software and hardware) to support advanced analytics
• Collaborate with GD colleagues to help them approach AI/ML more effectively
• Establish rigorous validation frameworks for AI models and monitor existing models for accuracy and efficiency
• Stay up to date with the latest advances in the field and, as appropriate, evaluate them for adoption at Regeneron

Senior Manager – Artificial Intelligence, Global Development

Research Scientist

• Set and refine quantitative biomarker strategies across multiple programs, aligning with Precision Medicine Strategy Leads and senior stakeholders.
• Translate program objectives into testable hypotheses, analytical roadmaps, and decision criteria that inform clinical development and asset strategy.
• Architect exploratory analyses of multi-modal datasets (genomic, transcriptomic, proteomic, metabolomic, clinical, and other biomarkers) to generate actionable insights.
• Define and review statistical frameworks, including hypothesis testing, modeling approaches, and power/sample-size analyses, ensuring appropriate interpretation.
• Oversee the correct application of statistical models on integrated datasets and drive clear, decision-oriented interpretation for translational and clinical teams.
• Contribute to the vision for scalable, reproducible pipelines and automated workflows that support enterprise-wide biomarker discovery and clinical development.
• Direct the design and enhancement of computational workflows for novel biomarkers; evaluate, integrate, or build tools as needed.
• Provide guidance on data cleaning, integration, and visualization standards to enable robust, interpretable analyses.

Principal Scientist – Quantitative Translational Scientist

Director

• enhance and improve interactions with key external US rare disease thought leaders at academic centers and leading community practices
• act as a coordinated, single point of contact to resolve issues between the thought leader and their institution
• assist with on-label in-person key thought leader development and drive thought leader advocacy with approved decks and materials
• plan and implement thought leader engagements and senior executive encounters at local, regional and national conferences
• communicate with sales partners on conference presence and support a regional conference strategy
• help pull through contracting and training needs with speakers

Associate Director, Thought Leader Liaison – Rare Disease

• The DM will work closely with their Alliance partner counterpart(s) to ensure full cooperation and transparency
• The DM will work closely to ensure appropriate development and retention of key personnel within the district to continue to facilitate growth in the commercial organization
• The DM will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US

District Manager – Gastro

Engineer

• supports equipment selection, CMO selection strategy, management of equipment qualification and process validation activities
• provides floor support during operations of off-site manufacturing
• reviews process data to ensure operational consistency after the processes are successfully transferred
• assists with investigation and root cause determination and identifies/implements CAPA for manufacturing deviations
• trends process performance and collaborates with teams to establish/improve process capability

Drug Product MSAT Engineer

Payroll

• conducting payroll audits and reviews prior to Associate Director Approval
• working with accounting to ensure all payroll data required for month end is provided in a timely and accurate manner
• preparing and/or reviewing and inputting all administrative payroll data changes for processing of bi-weekly and monthly payroll
• working with other departments such as Comp & Bens and HRPB’s to ensure payroll data is correct and processed accordingly
• reconciling each payroll, reviewing all entries and forwarding for approval
• ensuring all tax information, reconciliations and payments are managed
• managing the internal inbox and responding to employees’ queries
• assisting with audit queries related to payroll
• performing other duties or projects as assigned by management

Temp Manager – Payroll

• Leading the imaging operational component of assigned clinical trials
• Collaboration and oversight of the external imaging vendor at the study level
• Coordinate and contribute to cross functional review of imaging-related study documents
• Ensuring study documentation is audit ready
• Collaborate with clinical study leads and cross-functional teams to manage start-up activities
• Assist with vendor selection, request for proposals, management, and performance tracking
• Collaborating with data management on BICR deliverable timelines

Associate Manager, Clinical Imaging Operations

• Own the strategic direction, governance, and operational management of all testing services across Regeneron
• Lead a team of testing consultants distributed across the United States, Canada, and India
• Define and implement the enterprise MTS roadmap aligned to IT and business objectives
• Establish and implement testing standards, frameworks, and procedures across the SDLC
• Drive continuous improvement via automation, AI/ML-based testing, and shift-left methodologies
• Provide strategic mentorship on IT quality and testing optimization to senior leadership
• Negotiate contracts, pricing models, and resource allocation to optimize value
• Lead performance reporting, SLA compliance, and development of new SLAs/metrics as services mature
• Act as the primary communicator for all MTS topics, ensuring visibility and alignment
• Provide regular executive reporting on testing performance, risk posture, quality metrics, and service provider health

Associate Director – Service Delivery Management

• engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography
• conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews
• embrace a customer-centric, needs-based approach to drive strategic thought leader engagements
• coordinate thought leader engagements for senior executives at local/regional/national conferences and/or during day-to-day business
• develop/maintain list of key thought leaders in the assigned geography
• assist with thought leader development
• support speaker bureau buildout efforts
• share insights gleaned from interactions with thought leaders with Marketing and other functional groups
• support regional/national advisory board planning efforts

Associate Director, Thought Leader Liaison

• serve as a scientific and medical resource
• collaborate closely with internal and external stakeholders
• engage with leading experts and support clinical and research initiatives
• build positive relationships with key opinion leaders
• present clinical and scientific data to healthcare professionals
• support the development and management of company-sponsored and investigator-initiated studies
• gather and share relevant clinical and competitive intelligence from medical conferences
• ensure compliance with company policies while maintaining integrity in all interactions

Associate Director – Field Medical Affairs

Implementation Specialist

• Overseeing trial-level recruitment and retention tactics across assigned studies
• Collaborating with study teams to deliver compliant recruitment plans before FPFV
• Coordinating with Clinical Trial Management on milestones and country allocations
• Managing specialist vendors, tracking KPIs, compliance, and contractual delivery
• Reviewing and improving recruitment materials, content, and design elements
• Monitoring performance metrics and pivoting strategies based on emerging data
• Maintaining tracking systems, checklists, and recruitment process documentation