Software Engineer

• Provide end-to-end automation engineering support for the Rahway, NJ FLEx Center
• Ensure the reliable and compliant operation of process automation and OT/IT systems
• Support the successful implementation of automation solutions, including both platform technologies and associated reporting needs
• Execute / develop appropriate system validation, change control and user test acceptance documents (UAT)
• Maintain automation systems in a validated state, as part of an active/ongoing lifecycle management program and in compliance with Current Good Manufacturing Practices
• Troubleshoot challenging equipment/automation issues to improve equipment/automation system performance to support PSIM readiness

Associate Specialist, Engineering

Director

• Drive Quality Systems Transformation initiatives focused on deviation management, CAPA effectiveness, change management, quality risk management, and data governance.
• Strengthen standardization and continuous improvement of global quality system processes to ensure consistent application, transparency, and inspection readiness.
• Establish and reinforce master data management and data integrity controls that underpin right-first-time execution and regulatory confidence.
• Provide quality system expertise to ensure processes remain in a state of control, compliant with global regulatory requirements and internal standards.
• Act as a change agent to enable durable quality system and quality culture improvements through system-level rigor, governance, and traceability.
• Partner cross-functionally with site and functional teams to identify systemic gaps, influence adoption of global standards, and implement sustainable solutions.
• Support management oversight activities by developing and monitoring quality system metrics and key performance indicators.
• Author, review, and approve quality system documentation and governance materials in accordance with established procedures.
• Maintain expert-level knowledge of GxP requirements, regulatory expectations, and industry trends, providing interpretation and guidance to stakeholders.

Associate Director, Quality Systems

Clinical Research

• Planning and executing clinical-trial biomarkers across the pipeline
• Ensuring compliant, efficient biospecimen collection, assay execution, and data delivery
• Driving operational excellence, data quality, and compliance across the biomarker assay project lifecycle
• Partnering closely with scientific and operational colleagues to support a cohesive and agile team that delivers high-quality biomarker data for clinical trials and translational research
• Collaborating closely with biomarker scientists and study teams to plan clinical-trial biomarker set-up and logistics
• Serving as the operational partner to Biomarker Leads, helping implement strategies that advance biomarker programs
• Co-authoring biomarker-related sections of clinical study protocols
• Collaborating with Translational Molecular Biomarker Scientists to define and manage specimen collection, handling, shipping, storage, and processing requirements
• Developing biomarker vendor statements of work and data-transfer specifications in partnership with clinical teams
• Working with clinical teams to coordinate sample and assay logistics, issue resolution and risk mitigation
• Partnering with Data Management to transfer biomarker data from external vendors into the clinical data repository
• Designing sample collection kits, laboratory manuals, and specimen logistics for shipments to third-party vendors
• Building and maintaining effective partnerships with external biomarker vendors and internal teams
• Proactively identifying and resolving conflicting stakeholders needs to maintain alignment and momentum
• Implementing and continuously improving streamlined workflows that maximize efficiency and data quality

Senior Scientist, Clinical Research – Biomarker Operations

Marketing

• Develop and synthesize commercial data and insights for cross-portfolio priorities.
• Conceptualize and build set of analytics capabilities and tools anchored to our marketing and launch frameworks to support decision making for Global Vaccines portfolio and assets (e.g. market and competitor landscape assessment tools, Immunization eligibilities & vaccine hesitancy factors, benchmark libraries).
• Hands on analytics project delivery with expertise in data manipulation, analysis, and visualization using tools such as Excel-VBA, SQL, R, Python, PowerBI, ThoughtSpot or similar technologies and capabilities.
• Ability to leverage a variety of patient modeling techniques including statistical, patient-flow, and simulations-based techniques for insight generation.
• Partner with global marketing teams, DHH teams, and other cross-functional teams to inform strategic decisions and increase commercial rigor through all phases of pipeline asset development.
• Provide clear and synthesized communication to global marketing leaders and cross-functional teams, on commercial insights addressing the priority business questions.

Associate Specialist, Global Marketing Engagement

• Primary responsibility for strategy, oversight, and delivery of end-to-end activities involving new or marketed drug(s) for oncology indications
• Leads the team responsible for cross-functional delivery of critical milestones in an oncology asset’s lifecycle
• Creation, alignment, execution, and adaptation of the asset strategy cross-functionally
• Lead the asset development team to maximize the asset’s potential
• Identifying registrational opportunities for pre-clinical and early clinical candidates
• Evaluating pre-clinical and translational work for purpose of strategizing early clinical development plan
• Developing clinical development strategies for investigational or marketed assets
• Prioritizing clinical trials based on these clinical development strategies
• Support asset specific biomarker strategy and diagnostic readiness
• Support asset specific safety management
• Leading development and communication of the messaging around the asset and asset strategy
• Participation in internal and joint internal/external research project teams relevant to new compounds or marketed compounds
• Manage other Directors and/or Senior Directors on the asset development team
• Mentoring and career development for direct reports
• Work across teams and functions internally and/or externally
• Manage a complex matrix of internal stakeholders
• Travel on company business about twenty (20) percent of the time

Executive Director, Asset Development

Data Analyst

• Working collaboratively with Business, Operations, and IT stakeholders to ensure data management processes support key business use cases
• Processing the monthly formulary files which are required by the IAM organization
• Ensuring the files are delivered on time, execution of quality checks and processing overrides as outlined by IAM
• Coordination and processing of the annual frozen price data provided by IQVIA
• Management of market definition additions, changes and annual reviews that support Sales Reporting, Commercial Analytics and Contracting
• Market Definition processing for the Sales Force Automation (SFA) group requires an additional legal component that must be managed
• Hosting monthly meetings with business stakeholders to review upcoming changes and solicit all necessary approvals
• Management of the quarterly IQVIA diagnosis code file which is a pre-requisite for managing the internal indication and product mappings in support of Project Apollo which is used for Oncology related SIP activities
• Participation in all aspects of the Systems Development Lifecycle for GPM releases including providing business requirements, creation of user acceptance testing documents, execution of UAT and the production of all necessary documents
• Coordination with downstream consumers for testing is a requirement
• Maintenance of all GPM related documentation including SOPs (including an annual review), presentations, and website documentation
• Participation in product launch planning which requires attendance at weekly, bi-weekly, and monthly meetings, including the NDC Council
• Serve as the subject matter expert for the product data domain, supporting downstream consumers and their use of the product master data

GPM Data Analyst

Research Analyst

• Lead design and execution of equity‑centered RWD/RWE projects by therapeutic area that quantify disease burden, access, testing, treatment patterns, and outcomes across under‑represented populations.
• Develop mixed‑methods studies (EHR/claims analyses, registry data, SDoH integration, patient surveys, and qualitative interviews) and ensure outputs are timed to inform clinical programs, as well as relevant policy and commercial colleagues.
• Work cross-functionally to develop study protocols, statistical analysis plans, and methodological approaches that address selection bias, missingness in race/ethnicity/SDOH variables, causal inference, and subgroup inference.
• Integrate policy analysis into evidence generation: identify policy levers (e.g., Medicaid policy, payer coverage, reimbursement pathways) and translate study findings into policy recommendations.
• Manage strategic external collaborations and vendor relationships: identify and evaluate data partners, MSIs, FQHCs, safety‑net hospitals, community‑based organizations.
• Co‑lead co‑development of primary research with external partners (MSIs, FQHCs, community organizations) to ensure non‑extractive, trust‑based engagement and sustainable relationships that support recruitment and retention and post‑study continuity of care.
• Work closely with embedded/internal cross-functional partners to translate evidence into protocol design recommendations, site selection guidance, eligibility optimization, and outreach strategies.
• Produce actionable deliverables: TA‑specific, equity-centric RWD/RWE publications and plain language summaries and dissemination materials for both scientific and non‑technical audiences.
• Present findings to internal forums and to external stakeholders; publish in peer‑reviewed journals and present at scientific conferences.
• Mentor and build capacity across the HER Champion community; contribute to HER learning materials, SharePoint resources, and training modules.
• Ensure research adheres to ethical standards, privacy/regulatory requirements (HIPAA/GDPR where applicable), and community engagement best practices.

Health Equity Research Associate Director

Human Resources

• Serve as a trusted advisor to senior leaders across multiple organizations
• Coach leaders through complex and cyclical people processes
• Provide support for leader transitions, onboarding, and leader effectiveness needs
• Lead and support organizational design and alignment activities
• Drive talent and workforce planning aligned to a complex clinical development portfolio
• Provide day-to-day performance management guidance
• Collaborate across the HR network to resolve escalations and deliver integrated solutions

Associate Director, Human Resources Business Partner

Procurement

• Provide day-to-day support for global sourcing and contracting activities
• Support initiatives to optimize, standardize, and continuously improve sourcing and contracting processes and systems across global stakeholders
• Partner with business stakeholders to understand requirements and collaborate with the Digital Delivery team to translate needs into system enhancements
• Support implementation of global business process changes, including process documentation, testing, training, and change management activities
• Act as a central point of contact for procurement-related audits; coordinate documentation collection, analyze audit outcomes, and support self-audits to drive continuous improvement
• Support projects related to the maintenance, implementation, and ongoing enhancement of Corporate Policy 6 and related procurement policies and standards
• Provide operational support for key GSMG, GWES (Global Workplace & Enterprise Services_, and Supplier Development & Performance Management (SDPM) governance processes, including the Global Sourcing Committee, Grant of Authority (GoA), and annual company Corporate Audit & Assurance Services (MCAAS) audit programs.

Specialist, Procurement Process Excellence

Project Manager

• The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our Research & Development Division portfolio of clinical trials.
• GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally.
• The GCS Planning organization is the key interface between clinical development teams and the operational/executional arms within the business.
• The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level GCS point of contact representing the GCS Planning organization to customers both internal and external to GCS and serves as the lead GCS spokesperson at clinical and development related meetings.
• Working independently, the Program CSPM designs strategic and operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s).
• The incumbent must have demonstrated understanding of E2E product development process & connectivity between functions supporting pipeline (i.e. clinical development, CMC, supply chain, & human health), and balancing needs of patients & ensuring stable supply of product.
• Interacts closely with key partner organizations (as a lead GCS Planning program representative) such as clinical development, regulatory, quality and other supply chain areas to negotiate timelines, strategies and other related topics for all clinical supplies across all assigned program(s).
• Responsible and accountable for establishing the timelines for bulk manufacturing needs and release of drug product across assigned program(s).
• Works directly in the SAP system to establish a consolidated, visible forecast for all products used within the assigned program(s) (i.e. Bulk Drug Product).
• Oversees all bulk drug supply management and ensures proper allocation of drug product as needed across studies within assigned program(s).
• Responsible for identifying significant supply risks associated with clinical bulk activities in addition to serving in a lead role for clinical supply issue escalation within their program(s) (and subsequent manage thereof) to GCS Leadership.
• Responsible for the clinical supply budget for respective program(s) and for supporting all protocol and program cost estimates requested by Product Development Teams.
• Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to support critical CMC activities.
• Support the collection of clinical supply chain metrics and/or participate in critical non-pipeline activities as a subject matter expert in a particular area of expertise.
• Mentors new team members and supports staff development, as needed.
• Demonstrates high capability to solve unstructured problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and data
• Demonstrates ability to balance strategy with ability for tactical execution and has strong ownership & accountability of assigned work.
• Drive continuous improvement initiatives to enhance the efficiency, accuracy, and effectiveness of clinical supply planning processes and systems.
• Stay updated on industry trends, regulations, and best practices related to clinical supply planning and incorporate them into the team's operations.

Director, Global Clinical Supply Planning, Project Management

• Accountable for the development & execution of clinical supply plans for an assigned portfolio (Phase I–IV, IIS, collaborations)
• Ensures timely, compliant, and cost‑effective availability of IMP and comparators to support global clinical trials
• Leads a team of global clinical supply planners: recruits, deploys, coaches and develops staff
• Implements and standardizes planning processes and governance for the portfolio
• Builds and maintains working relationships with Clinical Operations, Clinical Research, Quality, Finance, Procurement, and external partners

Machine Learning Engineer

• Act as a trusted technical partner to DMPK scientists, clinical pharmacologists, statisticians, clinicians, and research leaders
• Facilitate cross-functional alignment, and translate scientific and operational needs into clear AI/ML solution requirements
• Design, develop, benchmark and deploy AI agents to support PDMB and clinical workflows
• Develop and apply machine learning and deep learning models for DMPK and clinical applications
• Define benchmarks and success metrics for AI agents and ML models
• Design and track value metrics such as time savings, cost avoidance, throughput improvements, and decision quality

Senior Scientist, Agentic AI, Machine Learning

• Leverage market and customer insights to shape market access strategies
• Develop payer customer segment strategies and promotional campaigns
• Identify opportunities and support appropriate pull-through activities and payer related solutions for field sales and account management teams.
• Monitor payer feedback and market dynamics to inform tactical adjustments to strategy
• Provide US payer input into Brand Marketing, Global Market Access Teams, new product planning, Integrated Account Management, Legal, Compliance, and Finance
• Active participation in the development of value evidence strategies; strong coordination with Outcomes Research / V&I (Value & Implementation Team)
• Support US Finance in development of segment level forecasts in support of brand forecast

Associate Director, US Pharma Payer Marketing

Data Scientist

• Lead deployment of advanced AI/ML solutions (multimodal transformers, graph or sequence models, Bayesian/probabilistic approaches) for toxicity prediction and translational safety applications
• Design and implement agentic AI systems tailored to toxicology use cases
• Specialize in the fine-tuning and alignment of foundation models for toxicology domain-specific applications and supporting new approach methods (NAMs)
• Drive collaboration with cross-functional teams of toxicologists, computational scientists, biologists, and chemists to ensure explainability, reproducibility, and address specific "context of use" regulatory requirements for safety assessments
• Champion best practices in model governance, and responsible AI within a regulated environment, helping to establish frameworks for responsible and ethical AI deployment in preclinical research
• Present and communicate science in key internal and external toxicology forums.

Senior Data Science Specialist

Account Executive

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MSD

Associate Specialist, Engineering

Associate Director, Quality Systems

Senior Scientist, Clinical Research – Biomarker Operations

Associate Specialist, Global Marketing Engagement

Executive Director, Asset Development

GPM Data Analyst

Health Equity Research Associate Director

Associate Director, Human Resources Business Partner

Specialist, Procurement Process Excellence

Director, Global Clinical Supply Planning, Project Management

Director, Global Clinical Supply Planning, Project Management

Senior Scientist, Agentic AI, Machine Learning

Associate Director, US Pharma Payer Marketing

Senior Data Science Specialist

Chronic Care Specialty Sales Representative