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Clinigen

Global pharmaceutical services and medicine access

Global Third-Party Risk & Compliance Manager

Regulatory Compliance & EthicsConfirmed live in the last 24 hours
Full-timeShah Alam, Selangor, MalaysiaNo salary listedIn-person

About the Job

Requirements

  • Experience in pharma, life sciences, healthcare services, or similarly regulated environments where third-party risk (anti-bribery and corruption, fraud, sanctions, and reputational risk) is material.
  • Experience using third-party due diligence systems and structured workflows such as RiskRate/NAVEX or comparable platforms.
  • Experience working with sanctions compliance expectations and controls, including screening, escalation, record-keeping, and programme components.
  • Familiarity with risk-based adequate-procedures expectations, including due diligence and monitoring and review principles, is beneficial.

Responsibilities

  • Own and maintain Clinigen’s global third-party risk management framework and operating standards, including scope, risk tiers, minimum due diligence requirements, escalation thresholds, and evidence expectations.
  • Ensure consistent application of the framework across regions and business units, partnering with Procurement, Legal, Finance, Quality, and operations to align onboarding and approvals.
  • Ensure the programme supports adequate-procedures expectations under global anti-bribery, sanctions, and financial crime frameworks.
  • Support remediation actions, conditions of engagement, and contractual controls when third-party risks are identified, working with Legal and Procurement.
  • Run the third-party compliance workflow in NAVEX RiskRate, including initiation, duplicate checks, questionnaires, screening outputs, risk decisions, approvals, and documentation standards.
  • Ensure third parties are not engaged before approval and stakeholders understand timelines and required inputs.
  • Drive continuous improvement to workflows, templates, and automation, and act as the business owner for enhancements needed to scale.
  • Ensure data quality, completeness, and consistency in the third-party system of record to support reporting, audit readiness, and decision-making.
  • Apply independent judgment and appropriate challenge when business urgency conflicts with third-party risk requirements.
  • Oversee initial risk screening and due diligence, ensuring review depth is appropriate to risk tier, including standard or enhanced due diligence when triggered by risk tiering.
  • Ensure third-party onboarding includes robust review of identity, ownership, location risk, services risk, and reputational indicators, and document findings in the system of record.
  • Manage go/no-go escalation when red flags exist and ensure decisions are risk-informed, consistent, and defensible.
  • Ensure third-party sanctions screening is performed and maintained, including appropriate escalation of potential matches and alignment with Clinigen sanctions requirements.
  • Support trade and export sanctions controls, including appropriate routing and escalation for sanctioned jurisdictions and commodity or Harmonized System code issues where required by policy.
  • Maintain clear records and audit trails for sanctions decisions and escalations.
  • Own the ongoing third-party screening and monitoring approach, including review, triage, resolution, and evidence of alerts as part of lifecycle management.
  • Ensure periodic refresh, re-screening, and re-due diligence when required, such as following risk changes, contract renewals, market expansion, or scope changes.
  • Support off-boarding and termination, and ensure controls prevent continued engagement with blocked or terminated third parties.
  • Produce third-party risk reporting for senior stakeholders, including pipeline volumes, aged cases, bottlenecks, high-risk concentrations, recurring red flags, and remediation themes.
  • Provide actionable intelligence to enable better business decisions, such as procurement interventions, process controls, and contract-gating improvements.
  • Provide targeted process enablement and practical guidance to business requestors and procurement and finance stakeholders on onboarding third parties correctly and avoiding retrospective onboarding.
  • Maintain clear user guidance and practical communications about third-party onboarding expectations.
  • Ensure appropriate hand-offs to Quality for GxP vendor qualification steps and align compliance approval with QA requirements without duplicating QA’s technical assessments.
  • Support a scalable, defensible third-party risk management capability aligned to Clinigen’s Ethics & Compliance programme, with duties evolving as business needs require.

Desired Qualifications

  • Familiarity with risk-based adequate-procedures expectations, including due diligence and monitoring and review principles.

About the Company

Clinigen

Global pharmaceutical services and medicine access

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.

Company size
501-1,000
Company stage
IPO
Headquarters
Branston, United Kingdom
Founded
2010

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