IT & Software

Associate Director, Program Data Lead

Novartis

London · Greater London · United Kingdom

Overview

In this role you will lead program-level clinical data strategy across multiple trials, acting as the Clinical Data Operations representative to align study execution with enterprise standards and regulatory expectations. You’ll influence cross-functional delivery, coach Study Data Leads, and shape data-driven development decisions to accelerate evidence generation. The position blends strategic leadership with operational oversight in a matrix environment, offering a meaningful impact on innovative therapies. This is a chance to drive Quality by Design and scalable data delivery within a global program.

Pay / Benefits
  • hybrid working options
  • minimum 14 weeks paid parental leave
  • performance-based bonus potential
  • insurance plans
  • retirement plans
  • wellbeing resources
Responsibilities
  • Lead end-to-end program-level clinical data strategies across multiple trials
  • Drive consistency in data collection, review, quality management, and delivery
  • Represent Clinical Data Operations on Global Clinical Teams and governance forums
  • Provide direction and development to Study Data Leads
  • Identify, assess, and escalate program-level risks and dependencies
  • Influence operational delivery strategies and integrate data considerations into development planning
  • Promote Quality by Design and lean, fit-for-purpose data collection practices
  • Partner with stakeholders to improve delivery predictability and stakeholder experience
Key requirements
  • Bachelor's degree in Life Sciences, Health Sciences, Data Sciences, Statistics, or related discipline
  • Typically minimum 10 years in clinical data management/operations within pharma/biotech/CRO
  • Experience leading multiple clinical trials or programs
  • Strategic oversight, risk management, and cross-functional leadership experience
  • People leadership, coaching, or team development experience preferred
  • Strong knowledge of clinical trial processes, data standards, and regulatory requirements
  • Understanding of quality management and risk-based approaches in development
  • Experience with program-level planning, governance, and execution
  • Ability to influence in a matrix organization without direct authority
  • Strong communication, negotiation, and stakeholder management skills
  • Strategic mindset with execution focus
  • Commitment to collaboration, continuous improvement, and talent development
  • Strategic mindset
  • Collaborative leadership
  • Stakeholder management
  • Clinical Data Management
  • Data Architecture Development
  • Data Governance

Reference: WJ-747_30239030

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