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Global Clinical Trial Manager

2 months ago

Reading, Reading, United Kingdom IQVIA Full time

Job Purpose

The Global Clinical Trial Manager is responsible for leading cross-functional clinical trial teams, guiding planning and management of assigned clinical studies from start to finish. This role requires proactive, iterative operational planning with effective contingencies and embedded risk management mindset in the team. The successful candidate will oversee budget and people allocation within assigned studies, contribute to promoting operational excellence through process improvement and knowledge sharing across studies, and foster an empowered, psychologically safe organization that can navigate a matrix environment, learn, and adjust quickly to changing conditions and business needs.

Key Accountabilities

  • Execute and deliver clinical studies, guiding planning and decision-making at the study level.
  • Act as the Clinical Trial Team product owner with clear and focused duties and responsibilities per the agile ways of working.
  • Active member of a Clinical Operations community within the study leadership organization.
  • Promote operational excellence in the development of global clinical study protocols, clinical study reports, and other study-related documents.

Deliverables

  • Patient recruitment, clinical data, study documentation, and study reports.
  • Efficient delivery of the protocol, ICF, Monitoring Plan, and CSR in quality and on time.
  • Cost-effective management of study budget.
  • Proactive, iterative operational planning with effective contingencies and embedded risk management mindset in the team.

Key Expertise and Skillset

  • Bachelor's degree in life sciences/healthcare (or clinically relevant degree) is required. Advanced degree is strongly preferred.
  • ≥ 4 years of recent involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV of standard to high complexity and priority.
  • ≥ 3 years of recent contribution to and accomplishment in all aspects of conducting clinical studies of standard to high complexity and priority (e.g., planning, executing, reporting, and publishing) in a global/matrix environment in pharmaceutical industry or a contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities.
  • Experience in managing people globally in a complex matrix environment preferred.
  • Management of virtual teams. Proven ability and strong experience leading teams and building capabilities.
  • Experience in developing effective working relationships with internal and external stakeholders.
  • Excellent communicator and presenter (oral and written); ability to communicate at all levels.
  • Excellent organization and prioritization.
  • Strong negotiation and conflict resolution skills and enterprise mindset, demonstrated by ability to drive for aligned solutions.
  • Fluent English, oral and written.

This role is not eligible for UK visa sponsorship.

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more.