Jobs at Johnson & Johnson

Serve as primary sponsor contact for assigned oncology trial sites. Manage site start-up, monitoring (on-site and remote), data quality, safety reporting, site supplies, training, recruitment support, CAPA, close-out, and stakeholder communication to ensure GCP and protocol compliance.

Lead and execute Real-World Evidence (RWE) studies end-to-end: design, data feasibility, extraction, cleaning, statistical analysis, programming, and interpretation. Develop shared tools and best practices, mentor team members, produce protocols and analysis-ready deliverables, and support regulatory interactions alongside therapeutic area scientists.

The Principal Data Scientist will lead the design of knowledge graph infrastructure in Immunology, standardizing and integrating extensive biomedical data for cross-functional analytics and insights. Responsibilities include data modeling, ontology curation, and collaborating with various scientific teams.

Lead clinical development and execution for late-phase neuropsychiatry programs (Ph2b/3), directing cross-functional teams, protocol design, safety/medical monitoring, regulatory submissions, publications, budget management, and mentorship of junior medical staff.

Lead translational pharmacology across aging and metabolism programs: drive target validation, assay development, candidate profiling, biomarker and PK/PD strategies, integrate human disease biology and clinical data to support candidate selection and early clinical translation, manage collaborations, and provide cross-functional scientific leadership and mentorship.

Lead design and implementation of ML, multi-objective optimization, GenAI and LLM solutions to support clinical trial operations (enrollment forecasting, cost estimation/optimization, site selection), perform stochastic enrollment simulations, harmonize clinical data, and communicate results to stakeholders while mentoring junior colleagues.

The Translational Post Doctoral Researcher will integrate multi-modal neuroscience data using AI, developing evaluation frameworks for drug discovery. Responsibilities include building data pipelines, assessing AI quality, and publishing findings.

Lead planning and execution of Knee Robotics R&D projects, owning scope, schedule, budget, EVM, RAID, change control, and cross-functional coordination (software, hardware, V&V, clinical, quality, regulatory, manufacturing). Drive design controls and phase-gate readiness, vendor coordination, launch readiness, stakeholder communications, and project closure activities in a regulated medical device environment.

Lead the Navigation software platform program across multiple projects, aligning roadmap, governance, release planning, risk mitigation, and cross-functional stakeholders in a regulated medical device environment. Drive platform-level decisions, financial planning, external partner oversight, release readiness, and executive reporting to ensure compliant, timely delivery of software-enabled surgical navigation and robotics solutions.

Lead development of RWD-driven analytics, ML/NLP/GenAI, optimization, and stochastic simulations to inform clinical trial design, feasibility, and execution. Build RWD cohorts, external controls, predictive models, and optimization engines; adapt LLMs for structured extraction; communicate insights to clinical and operational stakeholders and mentor colleagues on RWD methods and pipelines.

Postdoctoral scientist will develop and apply statistical and machine learning methods to analyze real-world and clinical trial data for neurology. Responsibilities include patient subtyping, disease-trajectory modeling, endpoint evaluation, robustness and bias assessments, integrating multimodal data, creating analysis-ready datasets and reports, and communicating results to cross-functional teams and regulators.

Lead vision and execution for medical imaging data products across ingestion, curation, integration, and consumption. Drive modernization of imaging pipelines and platforms, enable FAIR data governance and regulatory compliance, partner with therapeutic teams and vendors, and translate multi-modal imaging data into scalable clinical and business insights to support drug development.

Lead systems engineering for a complex surgical robotic platform: define architecture and requirements, manage risk and regulatory compliance, drive cross-functional integration, support V&V and design control, apply MBSE/UML, and enable product launch and post-market activities.

Lead planning and execution of Navigation platform R&D projects for regulated medical devices. Own integrated plans, budget/EVM, RAID, change control, and stakeholder communications. Coordinate cross-functional teams across software, systems, V&V, clinical, quality, regulatory, and manufacturing. Drive design controls, phase-gate readiness, hybrid Agile/hardware cadence, vendor delivery, project reporting, and closure activities to deliver scope, schedule, cost, and quality.

Lead cross-functional clinical teams to develop and execute late-phase (Ph2b/3) neuropsychiatry clinical development plans, oversee protocol design, safety/medical monitoring, regulatory submissions, clinical study reports, budget, and team management while interfacing with global stakeholders.

Plan, execute, and document verification and validation activities for robotic medical devices ensuring requirements traceability, regulatory compliance, and product safety. Develop V&V strategies, system test plans, automated and manual test methods, maintain test lab infrastructure, investigate failures, support regulatory submissions, and collaborate across systems, software, hardware, manufacturing, and quality teams to enable product release and launch.

Lead integration of target biology, computational protein design, cell engineering and experimental protein sciences to design and deliver immunogens and screening reagents for antibody discovery. Evaluate targets, define antigen and engineered-cell strategies, apply homology modeling and AI/ML design tools, optimize protein stability and expression, and enable hit-to-lead discovery across a global biologics discovery organization.

Manage advanced technology intake and execute cross-functional R&D projects for medical devices and robotics. Own integrated schedules, budgets, EVM, RAID, change control, and regulatory design controls. Prioritize pre-charter funnel, transition projects into NPD, coordinate software, systems, hardware and external partners, and lead/mentor engineering and PLM teams to ensure reliable, manufacturable, and compliant product development.

Lead development and deployment of imaging AI for oncology trials (CT/MRI/PET). Develop quantitative imaging metrics, automated segmentation, radiomics, and multimodal predictive models. Translate imaging-derived evidence into actionable clinical-development insights, collaborate with cross-functional teams and external partners, and publish scientific findings.

Lead a multidisciplinary systems engineering team to define system architecture, requirements, risk management, verification, and regulatory compliance for a safety‑critical surgical navigation platform. Drive cross‑functional integration across hardware, software, controls, clinical, manufacturing, and V&V to enable product development, regulatory submissions, and successful commercialization.