Johnson & Johnson

Data Scientist

• Design, develop, and validate statistical approaches and algorithms for patient stratification, leveraging both clinical trial and real-world datasets.
• Lead the statistical design, analysis, and validation of novel digital endpoints (e.g., wearables, speech, cognition) for neuroscience.
• Partner with our multidisciplinary team to ensure biological and clinical relevance of patient stratification strategies and novel endpoints.
• Apply rigorous statistical methodologies to algorithm development, ensuring reproducibility, robustness, and regulatory readiness.
• Develop and maintain statistical analysis plans, simulation studies, and innovative methodologies tailored to multimodal datasets.
• Apply advanced statistical and machine learning methods to large-scale datasets, including EHRs, claims, registries and longitudinal cohort studies.
• End-to-end expertise in RWE research including conceptualizing research questions, data feasibility, study design, analysis, programming, and interpretation.
• Communicate findings and methodologies clearly to scientific, clinical, and non-technical stakeholders.
• Contribute to regulatory submissions, publications, and presentations at internal and at scientific meetings.
• Stay current with emerging statistical methodologies, regulatory guidance, and best practices in RWE.

Director, R&D Data Science – Digital Health, Real-World Evidence, Neuroscience

QA Engineer

• Support Quality Systems including change control, supplier non-conformances, ASL management, Quality Agreements and department procedures and system, as assigned.
• Perform and Support supplier/ EM quality evaluations and/or audits, development of quality agreements, and other quality related activities impacting supplier.
• Lead activities associated with resolving supplier quality issues. This includes working with suppliers and internal partners to perform root cause analysis/failure investigations, identifying and implementing corrective actions, and monitoring for effectiveness.
• Lead activities associated with supplier risk management. This includes working with suppliers to identify areas of high risk within their processes; establishing, monitoring and implementing supplier risk mitigation plans; participating in supplier risk management projects; and ensuring management awareness of risks, gaining support for mitigation efforts and tracking progress.
• Lead activities associated with supplier process improvement. This includes working with suppliers to identify sources of variation within their processes; implementing process controls to improve process capability; and driving implementation of best practices.

Staff Supplier Quality Engineer

Operations

• Responsible for the development and execution of the clinical development plan
• Leads Cross-functional Clinical Team; supervises, develops and recruits junior medical staff
• Responsible for the oversight of medical monitoring/reporting and safety activities
• Responsible for overseeing content for the Independent Data Monitoring Committee (IDMC) and adjudication meetings as needed
• Prepares results of product research in preparation for global health authority submissions
• Assists Regulatory Affairs in the development of drug/device regulatory strategies
• May act as company spokesperson regarding publication of clinical research findings
• Helps explore and evaluate new product ideas

Senior Director, Clinical Leader – Neuropsychiatry

• Implement SQ strategy and follow Supplier Quality standards
• Manage Supplier related Non-Conformities (NC and SCAR's) and Corrective and Preventive Actions (internal CAPA's)
• Oversee supplier change requests (SCR) with Procurement
• Support Process Validations at suppliers
• Support QE with supplier product PVE's (First Article Inspection, Control Plans, Critical to Quality, Capability studies)
• Contribute to product investigations related to SCAR internal CAPA
• Support supplier preparation for inspections by authorities / third parties
• Support Procurement executing supplier transfer projects
• Support for Quality Agreement and Change Agreements, supplier assessments and supplier audit process
• Prepare regular report and supplier quality metrics
• Lead or participate in Quality projects: Legacy review, remediation, integration
• Implementation of improved/new standards for supplier quality
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures

Senior Supplier Quality Engineer

• Develop and maintain an AI governance roadmap that supports R&D strategy, enabling informed decision making and proactive management of AI related risks.
• Develop, implement, and drive adoption of quality assurance processes for AI/ML and GenAI development, integrate those processes with existing medical product and digital health tool development processes, and ensure adherence to internal and external regulatory standards.
• Drive alignment on AI quality/governance initiatives across R&D and enterprise, partnering with JJT to streamline governance workflows and promote consistent adoption across R&D.
• Create and disseminate playbooks, toolkits, and standardized guidance to support teams in implementing responsible AI practices.
• Establish and track metrics to evaluate governance effectiveness, including processes for audits, reviews, and risk based assessments of AI systems.
• Serve as a technical and strategic advisor on AI governance topics
• Collaborate with therapeutic areas, functional partners, and senior stakeholders to drive cross functional collaboration and alignment.
• Represent Johnson & Johnson in external AI governance forums and consortia, contributing to industry wide standards and best practices.

Associate Director, AI Quality and Governance – R&D Data Science, Digital Health

Sales

• Provide day-to-day support for all aspects of corporate cell phones, on/off-boarding, Vendor Credentialing and SAFE Fleet processes for J&J MedTech Surgery to field sales associates, other departments as required, and internal and external business partners.
• Support the overall planning, communication, revisions, and execution of policies and procedures for the field sales organization.
• Train and educate new hires on the corporate cell phone plans, Vendor Credentialing, and SAFE FLEET.
• Provide support for SAFE FLEET requests to field sales associates, other departments as required, J&J Corporate SAFE FLEET Management and external business partners.
• Manage accident investigation reporting system and assist in analysis of reports to help determine protective and preventative measures.
• Track and monitor SAFE Fleet Ambassador and SAFE Fleet Awards Programs.
• Initiate, develop, and analyze data/reports to provide insights for decision making and management updates.
• Support continuous improvements in current processes and create new capabilities to meet future needs.
• Provide support to Lead Analyst with activities as the need arises.
• Will report directly to the Director, Sales & KAM Effectiveness Administrator for all aspects of Health Care Industry Representative (HCIR) credentialing. This includes supporting the overall planning, communication, revisions, and execution of policies and procedures for HCIR credentialing.

Senior Analyst, Sales Enablement

• Design, develop, and validate statistical approaches and algorithms for patient stratification, leveraging both clinical trial and real-world datasets
• Lead the statistical design, analysis, and validation of novel digital endpoints (e.g., wearables, speech, cognition) for neuroscience
• Partner with our multidisciplinary team to ensure biological and clinical relevance of patient stratification strategies and novel endpoints
• Apply rigorous statistical methodologies to algorithm development, ensuring reproducibility, robustness, and regulatory readiness
• Develop and maintain statistical analysis plans, simulation studies, and innovative methodologies tailored to multimodal datasets
• Apply advanced statistical and machine learning methods to large-scale datasets, including EHRs, claims, registries and longitudinal cohort studies
• End-to-end expertise in RWE research including conceptualizing research questions, data feasibility, study design, analysis, programming, and interpretation
• Communicate findings and methodologies clearly to scientific, clinical, and non-technical stakeholders
• Contribute to regulatory submissions, publications, and presentations at internal and at scientific meetings
• Stay current with emerging statistical methodologies, regulatory guidance, and best practices in RWE

Director, R&D Data Science – Digital Health, Real-World Evidence (RWE), Neuroscience

• Provides overall quality assurance leadership in the management of select contract manufacturing sites and raw material suppliers engaged in the production of Johnson and Johnson products.
• Maintains the qualification of suppliers and their processes as well as lead activities associated with resolving complex technical issues that may require the development of new or improved techniques or procedures.
• Support Quality Systems including change control, supplier non-conformances, ASL management, Quality Agreements and department procedures and system, as assigned.
• Perform and Support supplier/ EM quality evaluations and/or audits, development of quality agreements, and other quality related activities impacting supplier.
• Lead activities associated with resolving supplier quality issues working with suppliers and internal partners to perform root cause analysis/failure investigations, identifying and implementing corrective actions, and monitoring for effectiveness.
• Lead activities associated with supplier risk management working with suppliers to identify areas of high risk within their processes; establishing, monitoring and implementing supplier risk mitigation plans; participating in supplier risk management projects; ensuring management awareness of risks and tracking progress.
• Provide Quality Engineering support to suppliers including assessments, inspection technique support, verification/validation activities, CAPA and change management.
• Develop and report on supplier performance metrics.
• Participate in local site supplier quality meetings to ensure communication and alignment of quality initiatives.
• Responsible for communicating business related issues or opportunities to next management level.

• Implement SQ strategy and follow Supplier Quality standards
• Manage Supplier related Non-Conformities (NC and SCAR's) and Corrective and Preventive Actions (internal CAPA's)
• Oversee supplier change requests (SCR) with Procurement
• Support Process Validations at suppliers
• Support QE with supplier product PVE's (First Article Inspection, Control Plans, Critical to Quality, Capability studies)
• Contribute to product investigations related to SCAR internal CAPA
• Support supplier preparation for inspections by authorities / third parties
• Support Procurement executing supplier transfer projects
• Support for Quality Agreement and Change Agreements, supplier assessments and supplier audit process
• Prepare regular report and supplier quality metrics
• Lead or participate in Quality projects: Legacy review, remediation, integration
• Implementation of improved/new standards for supplier quality
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed

Pricing Analyst

• Building, implementing, and executing the optimal pricing strategy for Janssen’s EPG portfolio, driving value across key payer segments, and evaluating value based agreements.
• Interact with Senior Brand Leaders, SCG Leadership Team, Legal, HCC and Finance in the establishment and implementation of pricing and contracting strategies.
• Serve as a brand pricing lead by synthesizing customer, industry and competitive insights and intelligence to guide in developing channel and franchise pricing strategies.
• Ensure awareness of price as key component of the marketing mix at the gross and net level.
• Effectively work with all key stakeholders to drive alignment on the pricing strategies and how they impact business.
• Lead CPC (Contracting and Pricing Committee) discussions regarding pricing strategies with Legal, Finance, Contracting Administration, HCS, HCC (Healthcare Compliance) and other key stakeholders.
• Proactively conduct competitive analysis and evaluate the changing marketplace and proactively make recommendations on pricing strategies.
• Act as a pricing strategy lead on customer contract negotiations and discussions.
• Develop Innovative Pricing Strategies and programs to insure patient and provider access at a reasonable Gross to Net.

Associate Director, Pricing Strategy – VAP, EPG

• Responsible for the development and execution of the clinical development plan
• Ownership for the design of clinical trials and for the content of clinical study reports
• Leads Cross-functional Clinical Team; supervises, develops and recruits junior medical staff
• Responsible for the oversight of medical monitoring/reporting and safety activities
• Evaluates adverse events (pre and post-marketing) for relationship to treatment
• Responsible for overseeing content for Independent Data Monitoring Committee (IDMC)
• Interprets, reports and prepares results of product research
• Assists Regulatory Affairs in the development of regulatory strategies
• Acts as medical contact at company for global health authorities concerning clinical/medical issues
• Manages the budget for all project related clinical activities

Clinical Research

• Executes and leads clinical trials, ensuring compliance with timelines and study milestones.
• Oversees/drives feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company SOPs.
• May serve as the primary contact for trial sites (i.e., site management).
• Develops clinical trial documents (e.g., study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports).
• Ensures applicable trial registration (e.g., on www.clinicaltrials.gov) from study initiation through posting of results and supports publications as needed.
• Manages/coordinates ordering, tracking, and accountability of investigational devices and trial materials.
• Partners and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel.
• Interfaces with, collaborates with and is responsible for Clinical Research Associates (CRAs).
• Coordinates and supports the development and execution of Investigator agreements and trial payments.
• Is responsible for clinical data review to prepare data for statistical analyses and publications.
• May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need.
• Ensure site staff are trained, and the corresponding training records are complete and accurate at any time point during all trial phases.
• Ensure that all Adverse Events (AE)/Serious Adverse Events (SAEs)/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate.
• For AEs/SAEs, ensures that they are consistent with all data collected and with the information in the source documents.
• May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS), with collaborative relationships with all relevant Clinical partners and cross-functional partners (e.g. Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and Market Access, R&D, etc.), contributing to cross-functional alignment.
• May provide on-site procedural protocol compliance and data collection support to clinical trial sites.
• Independently solves problems arising during clinical study execution, and will seek guidance for more complex problems, as needed.
• Responsible for communicating business related issues or opportunities to next management level.
• Knows, understands, incorporates, and follows all applicable laws and regulations relating to J&J business activities, and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.
• May be asked to provide additional support for the trial team, as needed.

Senior Clinical Trial Specialist

Manager

• Mentor, develop and lead a team of field-based Neuroscience Sales Specialists who will plan and implement territory business plans for breakthrough products
• Demonstrating business and clinical expertise while building a strategic plan and guiding the team to deliver sales results within an assigned budget
• Pull-through region / district vision, create team culture, manage representative performance, develop and motivate people and teams, demonstrate core product's clinical attributes, forge valuable customer relationships, and achieve sales quota
• Connecting and collaborating with internal and external customers and crafting our business to help the appropriate patients
• Working in the field with minimal direction, adapting quickly to change and demonstrating an understanding of pharmaceutical/biotech regulatory and promotional guidelines

Senior District Manager, Mood

• Develop and maintain a comprehensive understanding of the Copilot architecture, with particular emphasis on data management, privacy, and security protocols.
• Collaborate proactively with Business Technology teams to effectively communicate the benefits and functionalities of Copilot and Copilot Agents.
• Demonstrate expertise in the architecture of Copilot Agents, including integration with Graph API and the Microsoft Power Platform.
• Design, develop, and execute Proofs of Concept (POCs) to evaluate whether solutions meet business needs and are feasible.
• Contribute to the development of governance frameworks for Copilot Agents, ensuring adherence to compliance standards and responsible AI practices.
• Engineer prompts and workflows that are tailored to specific business scenarios, thereby optimizing Copilot and agent performance and value delivery.
• Provide technical support by troubleshooting issues and maintaining comprehensive documentation to support enterprise-wide deployments.
• Collaborate with cross-functional teams to establish processes for provisioning Power Platform Environments, ensuring Copilot Studio DLP Policies are properly implemented.
• Work closely with stakeholders to develop and manage a comprehensive inventory of Copilot Studio Agents, related environments, DLP Policies, and licensing.
• Partner with colleagues to identify and quarantine unauthorized Copilot Studio Agents, maintaining a secure and compliant environment.
• Contribute to the implementation of agent lifecycle management processes, supporting ongoing effectiveness through teamwork and shared responsibility.
• Foster and grow a Copilot end user community using Viva Engage and other adoption channels.

Director, R&D Data Science – Digital Health, Real-World Evidence, Neuroscience

Staff Supplier Quality Engineer

Senior Director, Clinical Leader – Neuropsychiatry

Senior Supplier Quality Engineer

Associate Director, AI Quality and Governance – R&D Data Science, Digital Health

Senior Analyst, Sales Enablement

Director, R&D Data Science – Digital Health, Real-World Evidence (RWE), Neuroscience

Staff Supplier Quality Engineer

Senior Supplier Quality Engineer

Associate Director, Pricing Strategy – VAP, EPG

Senior Director, Clinical Leader – Neuropsychiatry

Associate Director, AI Quality and Governance – R&D Data Science, Digital Health

Senior Clinical Trial Specialist

Senior District Manager, Mood

Manager – Microsoft Copilot, Copilot Agents