Johnson & Johnson

Director

• Design and conduct analyses that align to payer (e.g. CDA, NICE, HAS) and regulatory evidentiary requirements and fully leverage available data sources.
• Lead the design and execution of indirect treatment comparisons (e.g., MAIC, STC, NMA, ML-NMR), observational studies, and comparative effectiveness analyses.
• Provide expert guidance on statistical methodologies and programming approaches to address key research questions in collaboration with therapeutic area experts.
• Lead end-to-end delivery of evidence-generation workstreams, including systematic literature reviews, feasibility assessments, protocol development, statistical analysis plans, and technical reports/publications.
• Apply advanced statistical methods such as regression modeling, mixed-effects models, survival analysis, propensity score methods, and non-parametric techniques in accordance with study protocols.
• Partner across internal functions (e.g., Global Market Access, R&D, Medical Affairs, Health Economics Modeling, Epidemiology) to develop evidence generation strategies that optimize HTA outcomes.
• Engage and collaborate with external partners, providing scientific and technical input to support joint research initiatives.

Associate Director, Global Market Access Analytics, RWE

Procurement

• Lead Supplier Relationship Management process with critical suppliers
• Ensure execution of category strategies in collaboration with key stakeholders
• Manage complex contracts approval and compliance
• Develop category strategy and business engagement
• Lead the process for NPI pipeline needs identification

Senior Manager, Procurement – Biologics Category

Sales

• Independently guide and assist surgeons in the operating room by providing clinical and technical support of orthopedic surgical cases
• Advance DPS sales by serving as sole Company representative to provide direct customer support by attending surgeries
• Troubleshoot and apply independent judgment to respond to physician needs
• Share key customer, procedural and marketplace insights with other sales, clinical, marketing, and strategic account teams
• Prepare sales reports and documents as the need arises
• Provide Operating Room and Sterile Processing Department consultation
• Ensure all promotional materials are maintained in a presentable manner

Regional Clinical Sales Specialist – Orthopaedics

• Drive and/or support all aspects of spend performance
• Lead the SRM process with critical suppliers at senior executive level
• Ensure execution of category strategies in collaboration with stakeholders
• Manage complex contracts approval, administration, and compliance
• Develop and drive the category strategy in collaboration with internal partners
• Lead the process to identify the needs of R&D pipeline for material choices

Senior Manager, Procurement – Biologics

• Fulfill sales strategies by selling current and potential new oncology therapeutics
• Demonstrate a working knowledge of the product's clinical efficacy
• Articulate a value proposition for the customer, provide clinical support/information as needed, and achieve their sales objectives
• Conduct business analysis, actively prospect for new business within assigned accounts and call plan direction
• Develop account strategies with District Manager (i.e., identifies key accounts, develops specific plans for penetration)
• Develop customer-specific pre- and post-call plans that include objectives, probes, and supporting approved materials
• Optimally penetrate new and current accounts to increase sales in the assigned territory
• Appropriately apply all marketing tools and resources

Senior Oncology Sales Specialist, Solid Tumor

• Identify and evaluate cutting-edge external science across Immunology and immune-mediated diseases, from discovery through early clinical stages.
• Shape external innovation strategy aligned with Johnson & Johnson’s Immunology Therapeutic Area priorities.
• Serve as a scientific ambassador for J&J within global academic and biotech ecosystems.
• Lead global landscaping and AI-enabled search.
• Apply AI-driven and data-enabled approaches to discover, prioritize, and assess emerging science, platforms, and assets.
• Manage an effective engagement plan to ensure no strategic opportunity is missed.
• Lead or contribute to scientific diligence for collaboration, licensing, venture, and incubation opportunities.
• Build and lead external collaborations by developing trusted relationships with academic leaders, entrepreneurs, and biotech innovators.
• Collaborate closely with External Scientific Innovation (ESI), Business Development, R&D, JJDC, and GCSO leaders.

Director, Immunology – Scientific Innovation

Financial Planning and Analysis

• lead financial planning and analysis for Innovative Medicine
• managing Global Commercial Technology budgets
• optimize investment decisions and manage approximately $0.5B in technology spend across Operations IT and Business IT
• Provide budgeting leadership to support business partners for forecast updates, and quarterly/full-year processes
• Lead FP&A activities including forecasting, reporting, and strategic planning for technology investments
• Deliver actionable financial insights to influence decisions on capital allocation and cost optimization
• Partner with JJT partners, Portfolio team and JJT Finance teams to deliver strategic initiatives and support SigniFi adoption
• Manage a team of 4 analysts, fostering talent development and performance excellence
• Drive continuous improvement through process automation, benchmarking, and value stream mapping
• Ensure compliance with financial policies and governance standards
• Standardize accounting and reporting through consistent guidance and training
• Act as the liaison for JJT partners and finance teams across Commercial Regions
• Support ongoing global JJT ad hoc requests

Finance Manager

Field Engineer

• Manage the customer support system in the installation, service and repair of all products.
• Perform Technical Support to internal and external customers through the Customer Support Call Center.
• Manage account schedule and perform the installation, operation, repair and upgrades of equipment within assigned territory.
• Devises and implements preventative maintenance programs and maintains performance and service records for equipment.
• Responds to customer requests for emergency service, troubleshoots and takes corrective action.
• Provides guidance to customers and assists when customer satisfaction issues arise.
• Completes paperwork, documentation and administrative tasks per policy and procedures.
• Manage allocated inventory and complete required audits to support thereof.
• Complete all processing of RMA returns to support individual usage of parts and equipment.
• Support installation and support of products in clinical trials, external evaluations, regulatory testing or similar.
• Be familiar and adhere to J&J environmental and safety policies and guidelines.

Field Service Engineer, Orthopedics

Manager

• Mentor, develop and lead a team of 8-10 individuals towards attaining brand objectives for Gastroenterology products within the JJIM portfolio
• Demonstrate the ability to shape their business strategically while operating within an assigned budget
• Pull-through Immunology culture tenets, manage APP Specialist performance, develop and motivate people and teams, demonstrate core product's clinical attributes, forge valuable customer relationships, and achieve their brand objectives
• Collaborate with partners and work in the field with minimal supervision
• Completion of all required field standards, including timely and accurate documentation of customer engagements, expense reporting, and required trainings

Regional Business Manager, Advanced Practice Provider, Gastroenterology/IBD

Data Scientist

• Drive enterprise aligned AI governance across Data Science & Digital Health (DSDH) and the broader R&D organization
• Implement high quality, compliant, and scalable governance practices for both traditional AI/ML and GenAI systems
• Partner closely with DSDH teams, Quality, Legal, Global Regulatory Affairs, and Johnson & Johnson Technology to streamline governance processes
• Embed AI safety protocols and align with enterprise strategic priorities
• Develop and maintain an AI governance roadmap that supports R&D strategy
• 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
• 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
• Represent Johnson & Johnson in external AI governance forums and consortia

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

• Collaborate in the development and application of advanced AI/ML methods, including cutting-edge computer vision techniques applied to ophthalmic imaging data (e.g., Optical Coherence Tomography and fundus images), to uncover disease mechanisms and identify novel biomarkers.
• Collaborate in the development and validation of novel digital endpoints.
• Engage with regulatory stakeholders to ensure these innovations enhance clinical trial design, improve patient monitoring and care pathways, and meet regulatory requirements.
• Develop and apply sophisticated statistical models using real-world and clinical data to generate insights into disease progression, treatment outcomes, and patient stratification.
• Leverage longitudinal disease modeling, Bayesian methodologies, and causal inference techniques to inform decision-making.
• Apply emerging generative AI approaches to boost data analysis and knowledge discovery, integrating diverse multimodal datasets (imaging, clinical, wearable, etc.) for a more holistic understanding of ophthalmic diseases.
• Partner with Clinical Development and Medical Affairs to integrate RWE into evidence generation strategies.
• Support trial optimization and regulatory submissions by incorporating insights from large-scale clinical datasets, electronic health records (EHRs), and other real-world data sources.
• Build strong cross-functional collaborations within the company and spearhead external partnerships with academic institutions, technology providers, regulators, and industry consortia.

Associate Director, R&D Neuroscience Data, Data Science & AI – Ophthalmology

• We are seeking a visionary Director, R&D Neuroscience Data, Data Science & Artificial Intelligence – Ophthalmology to join the Neuroscience Data, Data Science & Artificial Intelligence (DDSAI) team.
• This leader will shape and execute innovative strategies leveraging multimodal data sources, digital health technologies, computer vision, artificial intelligence (AI), and clinical/real-world evidence (RWE) to accelerate drug discovery and development, and maximize patient impact.
• By combining ophthalmology expertise with strong data science acumen, this role will enhance clinical trial execution and ensure that new solutions are patient-centric and ready for regulatory and payer acceptance.
• As an integral member of a highly matrixed team, the Director will collaborate with cross-functional experts in the Neuroscience Therapeutic Area, Clinical Development, Quantitative Sciences, Regulatory Affairs, and Patient-Reported Outcomes, and forge strategic external partnerships to infuse new ideas and capabilities.
• This is a unique opportunity to redefine how we understand and treat eye diseases—uncovering novel digital biomarkers and endpoints, stratifying patients for more personalized care, and ultimately delivering better outcomes for people living with ophthalmic diseases.

Director, R&D Neuroscience Data, Data Science & Artificial Intelligence

Risk

• Actively participates in all study activities, contributing to the identification and assessment of key risks in the clinical protocol/set-up and advising clinical team members on effective mitigation strategies
• Participates in regular review of risk areas in collaboration with Risk Owners, to evaluate progress of risk mitigations and risk reduction, and to identify potential new risks or additional mitigation needs (trial and/or compound, as assigned)
• Maintains CQP (Clinical Quality Plans) in quality repository to facilitate regular progress reviews of quality support services in addition to risks and mitigations
• Collaborates closely with risk owners in evaluation of mitigation actions and effectiveness checks on mitigations
• Communicates and facilitates risk updates to R&D colleagues as part of the regular review cycle through Quality Working Groups and Governance Fora, as applicable (trial and/or compound, as assigned). Highlight new potential systemic risk to RDQ CRM management
• Develops and ensures a consistent interpretation of issues that require quality investigations
• Provides guidance for significant quality issues (SQI) per corporate standards and escalates SQI to senior R&D management
• Provides initial serious breach evaluation of quality issue that may require reporting to Health Authorities
• In collaboration with partners in RDQ, provides advice on the development and implementation of Corrective and Preventative Action (CAPA) Plans and Effectiveness Checks (Self - Identified, Inspection, Audit)
• Supports proactive inspection readiness activities throughout the study with trial teams to develop ongoing trial oversight, inspection narratives, identify and prepare sites of interest for inspection (including, pre-inspection visit support), ensures availability of key documents/records and coordinates mock inspection in collaboration with Regulatory Compliance teams.
• Provides support for Investigator, Sponsor-Monitor and third-party inspections including post inspection support
• Provides advice on questions related to research quality and compliance from Business Partners in collaboration with other Quality Professionals and Subject Matter Experts to ensure consistent interpretation of international regulations and policy.

Senior Specialist, Clinical Risk Management

Operations

• Lead and oversee activities to ensure the accuracy, completeness, and consistency of data.
• Act as a crucial link between business operations and IT, defining data standards, implementing validation rules, monitoring data health, and overseeing remediation efforts.
• Review data for errors, inaccuracies, or missing information.
• Generate regular and ad-hoc reports on data quality health, past issues, and improvement opportunities.
• Contribute to the definition of data quality policies, standards, and targets.

Manager, Data Quality Operations

• Capital Program creation and management
• Capital offer/deal development management
• Capital best practice creation, education, and training
• Contract Management liaison
• Prepare leadership team decks, content, and reporting
• Consult with Marketing on brand business plans