Director, R&D Data Science, Data Products - Global Development

Johnson & JohnsonTitusville, NJ
30dHybrid

About The Position

Johnson and Johnson Innovative Medicine (J&J IM), a pharmaceutical company of Johnson & Johnson is recruiting for a Director, R&D Data Science, Data Products - Global Development. This position has a primary location of Titusville, NJ but is also open to Spring House, PA or Cambridge, MA. This position requires up to 25% travel. About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine Position Summary The Director, Data Products - Global Development is responsible for leading the strategy, design, and delivery of user-centric, reusable data products that enable advanced analytics, data science, and AI/ML solutions across the Global Development organization. This role ensures that high-value internal and external development data assets-including protocol, study design, operational, regulatory, disclosure, and real-world data (RWD/RWE)-are standardized, productized, and integrated into Janssen's enterprise R&D data ecosystem. Working closely with Global Development Data Science teams, Clinical Development, Operations, and Regulatory stakeholders, as well as the broader Data Strategy & Products organization, this leader ensures that Global Development data products are AI-ready, semantically consistent, and interoperable, enabling trial efficiency, regulatory readiness, and improved compliance outcomes.

Requirements

  • PhD or Master's in informatics, computer science, life sciences, or related discipline.
  • 8+ years of experience in pharma/biotech R&D with focus on clinical development, operations, regulatory, or data product management.
  • Strong track record in data product development, integration, or semantic modeling in a regulated domain.
  • Experience working with multi-modal development data, including clinical trial, protocol, operational, submission, and disclosure datasets.
  • Deep knowledge of Global Development processes, clinical trial design, and regulatory requirements.
  • Deep knowledge of data products, database design, data transformation/mapping.
  • Familiarity with metadata management, ontologies, knowledge graphs, and industry standards (e.g., CDISC, FHIR, ICH).
  • Strong leadership, collaboration, and communication skills, with ability to translate technical strategy into business/science value.
  • Demonstrated ability to influence stakeholders and drive adoption of new data capabilities across a complex organization.

Responsibilities

  • Lead a team to define and deliver data products addressing critical Global Development use cases (e.g., study startup, TMF metadata, operational KPIs, submission readiness).
  • Define and maintain a roadmap for Global Development data products, spanning protocol development through clinical trial disclosure.
  • Develop data products through agile delivery and FAIR data principles, ensuring scalability, interoperability, and reuse across Janssen functions and external partners.
  • Integrate internal and external Global Development data sources, including CRO-provided datasets, performance benchmarks, and regulatory datasets.
  • Contribute to the development and governance of a Global Development Ontology to enable semantic consistency across operational and regulatory domains.
  • Align Global Development Ontology with enterprise metadata standards and external frameworks (e.g., CDISC, HL7 FHIR,etc).
  • Partner with Knowledge Management, Data Product Architecture & Governance, and Master Data Management teams to ensure Global Development data products integrate seamlessly into enterprise ontologies, knowledge graphs, and catalogs.
  • Collaborate with Global Development stakeholders-including Clinical, Regulatory, Medical Writing, QA, and Safety-to co-create solutions that maximize the value of development data assets.
  • Interface with regulatory and compliance teams to ensure data products meet submission, disclosure, and transparency requirements.
  • Lead a cross-functional team of product owners, data engineers, and Global Development domain experts.
  • Establish governance models, agile delivery processes, and value-tracking metrics for Global Development data products.
  • Define and track KPIs to measure the impact of data products on study startup times, operational insights, and regulatory compliance.
  • Communicate product vision, roadmap, and value realization to Global Development leadership, Data Science teams, and executive stakeholders.
  • Champion data literacy and adoption within the Global Development organization.

Benefits

  • Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
  • Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
  • This position is eligible to participate in the Company's long-term incentive program.
  • Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation -120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year Holiday pay, including Floating Holidays -13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave - 10 days Volunteer Leave - 4 days Military Spouse Time-Off - 80 hours

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What This Job Offers

Job Type

Full-time

Career Level

Director

Industry

Chemical Manufacturing

Education Level

Ph.D. or professional degree

Number of Employees

5,001-10,000 employees

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