# [HCC] Senior Manager, Health Care Compliance, Innovative Medicine R&D – Japan & Korea at Johnson & Johnson

Johnson & Johnson is hiring a [HCC] Senior Manager, Health Care Compliance, Innovative Medicine R&D – Japan & Korea in Tokyo, Japan. Level rates it Little AI ●○○○; you can [apply on Johnson & Johnson](https://jobsbylevel.com/go/2f24fd05-61ba-4336-a6ae-9df2a00ddb66?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Chiyoda, Tokyo, Japan.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Chiyoda, Tokyo, Japan
- Posted: September 24, 2026
- Apply: https://jobsbylevel.com/go/2f24fd05-61ba-4336-a6ae-9df2a00ddb66?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=hcc-senior-manager-health-care-compliance-innovative-medicine-r-d-japan-korea-at-johnson-johnson-94b884

## Prepare for this job

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## Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Legal & Compliance Job Sub Function: Health Care Compliance Job Category: Professional All Job Posting Locations: Chiyoda, Tokyo, Japan Job Description: The Senior Manager, Health Care Compliance (HCC), Innovative Medicine R&D – Japan & Korea is the senior compliance adviser and accountable HCC lead for Innovative Medicine Research & Development activities across the two-country cluster. The role provides visible, independent and risk-based leadership that enables ethical, patient-centric and compliant execution of clinical development, External Scientific Innovation and related scientific activities. Working across two distinct legal, regulatory, industry-code and cultural environments, the position partners with senior R&D leaders and regional and global stakeholders to anticipate, assess and mitigate HCC risks; convert complex requirements into practical decision pathways; strengthen business risk acumen; and sustain effective compliance programmes in both markets. The role also provides leadership beyond the cluster through selected APAC and global initiatives, helping scale consistent approaches, insights and capabilities across the region. Key Responsibilities Strategic Compliance Partnership Serve as the primary HCC leader and trusted strategic adviser to senior Innovative Medicine R&D leadership in Japan and Korea, with particular focus on Global Clinical Operations and other relevant R&D and innovation functions. Set a coherent cluster HCC strategy and annual risk-based priorities aligned with global and APAC objectives while recognising the distinct business, regulatory and cultural context of each market. Engage early in business planning, portfolio priorities, clinical-development strategies and external collaborations so that compliance considerations inform decisions before execution. Provide clear, constructive challenge and practical advice that enables responsible innovation, smart risk-taking and timely business outcomes. Coach leaders and employees to embed Our Credo, ethical judgement, accountability and a culture of integrity into day-to-day decisions. Risk Assessment and Advisory Own the cluster-level HCC risk assessment and mitigation approach, integrating country-specific risks into a clear view of priorities, controls, accountabilities and residual exposure. Advise on higher-risk or novel matters involving clinical studies, investigator and site engagement, study equipment, clinical-trial agreements and payments, HCP/HCO and government-official interactions, patient engagement, grants and donations, third parties, scientific and commercial independence, external innovation partnerships and related R&D activities. Translate complex requirements into practical guidance and defensible decision pathways; ensure significant or precedent-setting matters are documented and escalated appropriately. Drive a proactive lifecycle approach to risk identification, mitigation, monitoring and remediation by embedding HCC considerations into business planning, study governance and operational execution. Establish and oversee risk mitigation plans, leading indicators and corrective and preventive

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