Regional Clinical Audit Director – EMEA

GSK

Lead regional clinical audit program at GSK ensuring compliance and quality across Europe, Middle East and Africa. Collaborate with teams to drive effective control measures and improvements.

Posted 7/29/2026full-timeRemote • 🇬🇧 United KingdomLead💰 PLN 393,750 - PLN 656,250 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading clinical risk-based audit programs while ensuring compliance with regulatory requirements. Proven ability to build and manage audit teams, interpret metrics, and develop strategic initiatives to enhance audit quality and effectiveness.

Highest-signal resume keywords

Clinical Risk-Based Audit LeadershipRegulatory Compliance KnowledgeTeam Development and CoachingProject Management SkillsStakeholder Influence and Negotiation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Audit Program DevelopmentRisk AssessmentTrend ReportingClinical Trials ExperienceInternal Operations AuditingThird-Party Supplier AuditingRegulatory InteractionInspection ReadinessPolicy and Procedure ImplementationMetrics Interpretation

Soft Skills

Interpersonal SkillsIndependent Decision-MakingCommunication SkillsPresentation SkillsNegotiation Skills

Industry Keywords

Life SciencePharmacyHealth ScienceScientific IndustryRegulatory RequirementsCross-Functional ManagementMatrix OrganizationGeographical BoundariesCompliance IssuesAudit Quality

About the role

Key responsibilities & impact

Lead design and delivery of a clinical risk-based audit programme across Europe, the Middle East and Africa that meets regulatory authority requirements leveraging different and novel audit types.
Build, lead and coach a team of auditors to deliver consistent, high-quality audits and effective follow-up.
Provide strategic input in the development, management, and implementation of strategies and initiatives, policies and procedures to support the audit program.
Build and maintain beneficial working relationships with internal and external customers and across the Matrix in R&D Quality and Risk Management.
Interpret metrics, trend reporting and insights to inform risk priorities and improve controls.
Support inspection readiness, regulatory interactions and investigations of significant compliance issues.

Requirements

What you’ll need

Bachelor’s degree in Life Science, Pharmacy, Health Science, or related discipline (or equivalent experience).
Scientific/pharmaceutical industry background with experience in clinical trials.
Knowledge of global, regional, and national regulatory requirements and regulations.
Experience delivering risk-based audits of internal operations and third-party suppliers.
Experience leading and developing audit teams across multiple locations.
Project management skills and management of complex cross-functional activities.
Verbal, written, and presentation skills and ability to influence and negotiate with senior stakeholders.
Ability to work independently and make decisions with minimal supervision.
Interpersonal skills, and ability to work in the matrix across geographical and organisational boundaries.

Benefits

Comp & perks

Competitive salary
Annual bonus
Share-based long term incentive program