Global Third-Party Risk & Compliance Manager
Clinigen
Global Third-Party Risk & Compliance Manager
Clinigen
Global pharmaceutical services and medicine access
Clinigen · Shah Alam, Malaysia · Full-time · Posted 2026-08-27
Workplace: on_site
Department: Support Functions
Clinigen’s third‑party ecosystem is wide and includes suppliers, service partners, consultants, distributors, and other intermediaries who can create ABAC, fraud, sanctions, reputational and operational risk if not properly assessed and controlled. This role provides the organisation’s front‑door integrity control: ensuring that third parties are vetted and monitored, risk is visible, escalations are handled consistently, and decisions are documented and auditable.
The role is also accountable for ensuring that third‑party due diligence is not a one‑off event — but a lifecycle process with ongoing monitoring and clear remediation steps, consistent with modern regulatory expectations
Key Responsibilities:
1) TPRM Operating Model Ownership (Global)
2) NAVEX RiskRate Platform Ownership (End‑to‑End)
3) Due Diligence & Risk Assessment (Proportionate, Risk‑Based)
4) Sanctions & Trade Sanctions Controls
5) Ongoing Monitoring & Lifecycle Management (Third‑Party Specific)
6) Third‑Party Risk Intelligence, Reporting & Insight
7) Stakeholder Enablement (Process Adoption Without Owning E&C Training)
8) GxP / Quality Interfaces (No Duplication of QA Vendor Qualification)
Additional Duties:
The above list is not exhaustive. Duties may evolve based on business needs, and the post‑holder is expected to work flexibly to support a scalable, defensible Third‑Party Risk Management capability aligned to Clinigen’s Ethics & Compliance programme
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Clinigen provides pharmaceutical services and medicines to help patients gain ethical access to treatments. It revives niche, hospital-only medicines and offers end-to-end services across the product lifecycle, including clinical trial supply, access programs, and global commercialization. Its three divisions—Clinical Services, Access and Commercialisation, and Lifecycle Services—work with pharma partners to manage regulatory affairs, pharmacovigilance, and market access across more than 100 countries for major pharma clients. The goal is to combine product revitalization with comprehensive lifecycle management to improve patient access worldwide.
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