Global R&D Director – Risk and Compliance
Job in
Weybridge, Surrey County, KT13, England, UK
Listed on 2026-07-19
Listing for:
Jobtailor
Full Time
position Listed on 2026-07-19
Job specializations:
-
Management
Risk Manager/Analyst, Regulatory Compliance Specialist -
Finance & Banking
Risk Manager/Analyst, Regulatory Compliance Specialist, Financial Compliance
Job Description & How to Apply Below
Responsibilities
- Ensure and enable a compliant organisation and robust inspection readiness across RDP
- Provide risk and compliance oversight, coordinating governance for risks owned or monitored by the R&D Head and CMO
- Act as a Centre of Excellence for Risk, Compliance and Management Monitoring across RDP and R&D
- Build, lead, coach and develop an efficient and motivated team
- Manage team budget, resources and operational activities
- Set, deploy and maintain meaningful KPIs and metrics
- Own and drive the management monitoring process
- Support RDP stakeholders in risk management
- Oversee the regulatory intelligence process for GVP, GCP and GLP regulatory requirements
- Establish and maintain appropriate risk management structures and processes
- Collect and consolidate relevant information from risk owners
- Coordinate risk management forums
- Act as the key contact point between Enterprise Risk & Audit and R&D functions
- Articulate and communicate risk management principles and frameworks across R&D
- Develop supportive materials to strengthen compliance and risk management
- Degree in Life Sciences or equivalent
- Minimum 15 years of experience in Risk, Compliance and Quality management within R&D functions
- Broad scientific or pharmaceutical industry background with strong experience across R&D environments
- Demonstrated project management capability, including management of complex cross-functional activities
- Strong data and KPI capability, including identifying relevant measures, analysing trends and producing meaningful reports and actions
- Experience using quality tools, risk management tools and relevant digital systems
- Experience supporting QPPV activities, including contribution to the Pharmacovigilance System Master File (PSMF)
- Experience establishing or maturing risk governance frameworks in matrixed global organisations
- Experience designing and delivering compliance or risk management training across diverse stakeholder groups
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