[Innovative Medicine]] R&D, Clinical Development Immunology TA, Clinical Lead

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•Japan Clinical Lead is responsible for development and execution of clinical development strategy for target indication in assigned compound to obtain regulatory approval in Japan
• Based on the Japan clinical development plan in alignment with global development strategy, Japan Clinical Lead is responsible for planning/execution/reporting of clinical studies and health authority interactions on clinical matters

Responsibilities for clinical development strategy in Japan

• Develops clinical development strategy of target indication which fulfills Target Product Profile (TPP)/target label and target New Drug Application (NDA) submission timeline.
• Develops clinical data package, designs local/regional studies or selects Global studies constituting the clinical data package.

Responsibilities in Global study

•Reviews study plan and design [i.e.

Protocol Element Document (PED)/protocol(s) or any relevant study design information].
•Assess clinical feasibility with local medical needs for Japan participation.

Provides input to global clinical team (CT) and compound development team (CDT).
•Request to create local amendment if needed to fulfil Japanese medical and regulatory needs.
•Develops clinical section on Clinical Trial Notification (CTN) and responds to clinical related queries from PMDA
•Partners with clinical operations for study setup and execution to ensure that the study is executed according to the protocol and required Japanese data can be obtained.
•Reviews study related documents including Japanese translated Investigator's brochure (IB) and Informed Consent Form (ICF) with clinical and scientific point of view.
•Participates in Clinical Functional Trial Team (CFTT) meeting or other relevant venue (detail tbd) for each study as Japan representative and provides inputs from Japan perspectives
•Provides medical monitoring support for Japanese participants if needed

•Executes safety monitoring and assessment as one of core members of J-SMT

Responsibilities in Local/regional study

•Designs study and develops PED/protocol(s)
•Establish Efficacy and/or Safety and/or Diagnosis Committee if needed
•Reviews study related documents including Statistical Analysis Plan (SAP)/Data
•Presentation Specification (DPS), materialsIDMC charter (if necessary), analytical riskbased monitoring plan, criteria of protocol deviation plan
•Develops clinical section on Cli...