OneTrust

Sales

• Be responsible for attaining sales objectives, presenting complex clinical and business information on JJIM's immunology products and services to an audience of office and institutional based Gastroenterology healthcare professionals, government agencies, professional and patient groups, health plans and others involved in the decision-making process.
• Use discretion and judgment to execute the franchise and company brand strategy and tactics within the assigned customer segment
• Influence decision makers and influencers within assigned customers to support the use of the company's products in the treatment of relevant disease states by developing and applying clinical and business expertise, and effective selling skills.
• Execute marketing strategies at the local level, leveraging resources appropriately and working successfully with company team members and counterparts to share ideas and information to enhance business results.
• Build customer loyalty by identifying and cultivating relationships with key decision makers at the local level who can influence decision making within the healthcare provider systems.

Immunology Sales Specialist, Gastroenterology

• Fulfill sales strategies by selling current and potential new oncology therapeutics.
• Demonstrate a working knowledge of the products' clinical efficacy, provide clinical support/information as needed, and achieve their sales quota.
• Conduct business analysis, actively prospect for new business within assigned territory.
• Develop customer specific pre- and post-call plans that include objectives, probes and supporting materials.
• Build customer dedication and identify and cultivate new relationships.

Oncology Sales Specialist

• Devise and implement customer specific pre and post call selling approaches.
• Consistently use approved clinical studies and marketing aids to support the case for the value proposition when selling.
• Position and adapt the message to meet the practitioner’s, institutions, and company’s objectives.
• Develop and execute on comprehensive business plan that includes opportunities and challenges in local market.
• Develop a territory coverage plan that maximizes selling time with all account professionals.
• Maximize and customize the value proposition and influence contract implementation processes.

Neuroscience Sales Specialist

Strategy

• Transform the CSS Supply Chain by leading a series of strategic initiatives.
• Ensure that the program delivers supply chain performance and processes.
• Partner with other Strategic Initiative leaders to support key program metrics.
• Develop and execute project governance and ensure delivery of overall program commitments.
• Proactively identify potential risk areas for the program and collaboratively mitigate.
• Lead design of future business processes for project completion.
• Ensure integration with key variables including demand/supply scenarios.
• Collaborate with functional business partners and supply chain teams for policy deployment.
• Support identification of additional opportunities to drive increase value and org efficiency and effectiveness.

CSS Director – Strategic Projects

Manager

• Assist with identifying research study needs, drafting proposals and protocols, and contributing to epidemiology study conduct across the clinical development program
• Assist with conducting fit for purpose database and study feasibility assessments and executing analyses across the product cycle
• Conduct literature reviews and synthesis; provide assistance to senior epidemiologists and clinical teams with study design; and identify and evaluate data resources to meet therapeutic needs
• Work closely with colleagues in the Observational Health Data Analytics group when defining research questions, developing epidemiological protocols, and implementing solutions
• Provide epidemiological and/or statistical consulting, education and support to product teams, and assist with disseminating technical information through technical reports, presentation, and publication in peer-reviewed literature
• Research natural history of diseases, both within and outside of existing electronic databases, to understand the inherent risks associated with the indication; statistical risk assessment; using historical clinical trial data and other observational databases to develop an understanding of potential safety issues for new medications, and indications, based on experience with related compounds
• May work in cross departmental/sector committees, and or other efforts supporting J&J Innovative Medicine
• Keep up to date with the FDA and other Regulatory Agencies regarding regulatory requirements for Post Approval Authorization Studies and Risk Management plans and the development of formal guidance for use of RWE for Regulatory Decision Making

Manager, Oncology Epidemiology

DevOps Engineer

• Collaborate with product developers, QA, and V&V teams to ensure safe, auditable releases.
• Incorporate industry standards and best practices to continuously improve our CI/CD pipeline.
• Implement and maintain build reproducibility, artifact provenance, and secure supply-chain controls.
• Troubleshoot and resolve complex DevSecOps issues across build, test, and release systems.
• Automate SBOM generation, management, and publishing for software and firmware builds to meet traceability and compliance needs.
• Automated OS image creation and vendor driver integration to ensure repeatable, consistent system images.
• Create product-specific installers using InstallShield.
• Owned and optimized product-specific Jenkins build pipelines for predictable releases.
• Provisioned and maintained VM build servers, build tools, and licensing for stable CI/CD environments.
• Manage software component configuration and dependency mapping.
• Integrate static code analysis and vulnerability scanning to surface issues earlier and strengthen security.
• Deliver faster, more reliable releases, reduce manual effort, and lower operational and security risk.
• Mentor engineers on CI/CD, build-system design, and secure-development practices.
• Maintain clear documentation for processes, runbooks, and environment configurations.

Senior Software Engineer, DevOps

• Developing core medical education content and coordinated programs directly and through the regional/country teams to elevate customer knowledge, confidence and rapidly embrace the JJV specialty contact lens (presbyopia, astigmatism, myopia management) portfolios in practice, and drive peer to peer advocacy
• Building and developing the global professional education strategy as well as supporting execution of professional plans in partnership with markets to drive category development and growth
• Compliant contracting and management of ECPs and KOLs to ensure regular insights, endorsement and support in the effective delivery of strategy/programs to achieve differentiation and JJV specialty contact lens portfolio recommendation
• Foster a high-performance environment and culture of collaboration and innovation
• Enable strong collaboration with cross-functional teams
• Develop regional capabilities to maximize global Digital Solutions assets to differentiate and enable delivery
• Leadership responsibility for assuring necessary tools, policies and procedures are developed and integrated to support and align with all legal, regulatory and Health Care Compliance policies

Manager, Global Medical Education – Specialty Contact Lenses

• Work closely with the Business Product Owner (BPO) and other stakeholders to understand evolving business needs, ensuring the solution aligns with scaling objectives and expansion for the use cases supporting key business processes.
• Collect feedback from users, stakeholders, and analytics to identify areas for improvement or new features that support scaling while maintaining user satisfaction.
• Work closely with Scrum Master/PM, Business Analysts, developers (Front-end and Back-end Data Engineers), UX/UI designers during iterations; clarify requirements and answer questions during sprints.
• Engage with stakeholders to get data and requirements for scenario runs and refresh/develop scenarios in DST as needed.
• Maintain a well-organized backlog of user stories, features, and fixes; ensure that the backlog is transparent and accessible to the team.

Manager, Digital Value Chain

Data Scientist

• Take a leadership role with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s).
• Gather and/or review content and integration requirements for eCRF and other data collection tools.
• Establish conventions and quality expectations for clinical data.
• Establish expectations for dataset content and structure.
• Set timelines and follow-up regularly to monitor delivery of all data management milestones.
• Review clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
• Ensure compliance with regulatory guidelines and the documentation matrix.
• Ensure real-time inspection readiness of all DM deliverables for the trial and participate in regulatory agency and J&J internal audits as necessary.
• Plan and track content, format, quality, and timing of applicable data management deliverables.
• Ensure deliverables are on time.
• Take a leadership role with the assigned clinical working group(s) to ensure that DM and TA trial needs and deliverables are achieved.
• Create key functional plans (e.g. study Integrated Review Plan) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
• Identify and communicate lessons learned, best practices, and frequently asked questions at the trial level.
• Identify and participate in process, system, and tool improvement initiatives.
• Perform trial level oversight controls and/or execute data management activities per applicable procedures, with DML direction.

Analyst II, Global Data Manager

Implementation Specialist

• Act as the primary point of contact for assigned implementations and own end-to-end delivery
• Collaborate with key stakeholders to develop process flows, requirements and program solutions that enhance patient, provider and agent experiences
• Ensure timely product development and implementation that meets PSC/PECS expectations
• Collaborate with PSC technology group to review system requirements that enhance the agent experience
• Facilitate conversations with operational teams to determine their needs and deliver solutions that optimize operational workflow
• Define project scope and translate it into actionable tasks and schedules
• Manage implementation processes, including progress tracking, problem resolution, system implementation, testing, documentation, and training
• Provide leadership to guide cross-functional teams toward project goals while maintaining quality and customer satisfaction
• Lead cross-functional teams to effectively plan project meetings and drive accountability for deliverables
• Update stakeholders on progress and manage expectations regarding project aspects
• Identify issues, explore solutions and implement effective resolutions
• Up to 25% travel is required

Implementation Manager

Operations

• provide expert reviewing, writing, and editing support to ensure timely production of high-quality documents (abstracts, posters, slide presentations, manuscripts, letters to editor, etc.) for publication in medical/scientific journals or presentation at medical/scientific meetings, and maintain compliance with all company policies/procedures and applicable industry standards/guidelines.
• Responsible for scientific publication writing including abstracts, posters/oral presentations, and manuscripts, etc., and responsible for the overall production of publications and compliance with standard operating procedures/industry standards.
• Familiar with the overall publication plan for product(s) and proactively fulfills Pub Ops’ role in generating assigned publications, including assigning medical writers and providing editing and project management to efficiently deliver high-quality publications to author teams.
• Has extensive knowledge of medical/scientific journals and congresses for assigned products and therapeutic areas.
• Partners with product team personnel (e.g., CDTL, GMAL, SEL, etc.) to advance publication-related goals of the team.
• May be involved with strategic/tactical planning for the submission and/or timing of publications.
• Organizes kick-off meeting with authors for development of publication.
• Provides direction, oversight and editing for contract medical writers and junior-level medical writers.
• Manage and/or review and interpret data and source documents for information required for publication.
• Assist in table and figure mock-up development.
• Actively engage internal and external authors and other key stakeholders in the development of publication plans and strategy at the individual dataset, study, and/or compound level.
• Participates as a member of Publication Teams and Product Teams, providing publication-related advice and input.
• Serves as a Subject Matter Expert (SME) on J&J publication policies and procedures, including but not limited to J&J Publications SOP, JPUBS, and applicable industry standards including Good Publication Practice (GPP), International Committee of Medical Journal Editors (ICJME) recommendations, CONSORT Guidelines, American Medical Association (AMA) Manual of Style, and Council of Biology Editors, etc.
• Assists in developing or updating publication-related SOPs and Guidelines.
• Participates in the development and maintenance of document templates, style guides, electronic document management and publication review and approval system.
• For encore abstracts/posters/oral presentations, partners with relevant stakeholders (e.g., GMAL, SEL, SCL, authors, writers) to efficiently deliver assigned encores.

Associate Director, Global Medical Affairs – Publication Operations

Director

• Own and lead the SAP S/4HANA transformation program: strategy, planning, governance, delivery, budget and risk management.
• Act as single-point program lead between business executives, process owners (Finance, Supply Chain, Manufacturing, Quality, Sales & Marketing, R&D), IT, external system integrators and vendors.
• Define and validate the target operating model, solution architecture, business process design and roadmap using SAP Activate or equivalent methodology.
• Drive blueprinting, configuration oversight, integrations, data migration strategy and execution, custom development prioritization and cutover planning.
• Ensure regulatory and quality requirements relevant to medical devices/orthopedics (e.g., traceability, quality management, auditability) are embedded into the solution.
• Lead the program delivery cadence: steering committees, executive reporting, program financials and milestone tracking.
• Oversee testing strategy (unit, integration, UAT, performance), deployment, hypercare and stabilization.
• Manage change management, communications, training and organizational readiness to drive adoption and benefits realization.
• Direct vendor/SI performance, contract deliverables, SLAs and coordinate internal shared services.
• Measure and report program outcomes vs. business KPIs and benefits (cost, lead time, quality, compliance, user adoption).

IT Director – ERP Transformation, Orthopedics

• Lead the strategy, design, and delivery of user-centric data products
• Ensure high-value regulatory data assets are standardized, productized, and integrated
• Collaborate with Global Regulatory Affairs teams to ensure data products are AI-ready, semantically consistent, and interoperable
• Define and deliver data products addressing critical Global Regulatory Affairs use cases
• Develop data products through agile delivery and FAIR data principles
• Contribute to the development and governance of a Global Regulatory Affairs Ontology
• Partner with teams to ensure data products integrate seamlessly into enterprise ontologies
• Define and track KPIs to measure the impact of data products on submission effectiveness and compliance risk reduction

Director, R&D Data Science, Data Products – Global Regulatory Affairs

Product Manager

• Drive the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area, their development plans and status and knowledge of labeling aspects for labeling development and target labeling for new products.
• Take a leadership role and partner with Global Regulatory Leads (GRLs) and other functional area partners (clinical, safety, market access, commercial, medical affairs) to ensure the global labeling strategy aligns with the Global Regulatory and Product Strategy for assigned products.
• Lead target labeling development.
• Collaborate with functional areas to provide labeling input relevant to clinical study protocols and ensure alignment on endpoints and Patient-Reported Outcomes (PROs), with a label-as-driver approach.
• Provide strategic labeling advice for local labeling in major markets.
• Analyze relevant competitor labeling, leverage labeling guidance and trends to develop labeling strategy and content, including risk and mitigation identification and assessment.
• Lead Health Authority (HA) labeling strategy discussions and development of contingency labeling plans and content.
• Lead the development, revision, review, agreement, and maintenance of target labeling, primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents) for assigned compounds.
• Lead cross-functional Labeling Working Group (LWG) and strategic labeling discussions leading to development of target and primary labeling.
• Represent global labeling in Global Regulatory teams and other cross-functional teams, as appropriate.
• Present at governance meetings, such as Labeling Committee, to seek endorsement of labeling.
• Provide advice and guidance about labeling content, processes, timelines, and scientific integrity.
• Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
• Ensure high quality and compliant labeling documents.
• Contribute to the continuous improvement of the end-to-end labeling process.
• Support global labeling inspections and audits for assigned products, as applicable

Associate Director, Global Labeling Product Leader

• Independently lead, manage, and mentor a multidisciplinary team of RWE scientists to influence strategy and execute on the priorities
• Partner with the Data Science Therapeutic Area leaders to conceptualize, lead, shape and deliver Real World Evidence.
• Be a hands-on scientific and technical leader, lead a portfolio of RWE projects, and develop best practices and a common suite of tools.
• Provide end-to-end expertise in RWE studies including conceptualizing research questions, data feasibility, study design, analysis, programming, and interpretation.
• Provide scientific leadership in developing and applying Real-World Data (RWD) methodologies to mitigate observed and unobserved biases.
• Provide thought leadership to generate actionable insights from historical trial data, observational databases, and literature reviews to support regulatory agency interactions.
• Independently create study protocols, analysis plans, and statistical programming deliverables including analytical dataset, tables and figures.