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ICON plc

RBSM - Lead

Regional Great Britain (Northern Ireland)
Posted about 23 hours ago
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RBSM Lead

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

The Role

As a Risk-Based Study Management Lead, you will provide end-to-end risk oversight for assigned clinical studies, ensuring risks to patient safety, data quality, and trial integrity are proactively identified, discussed, and managed throughout the study lifecycle. You will work in close partnership with the Clinical Research Manager (CRM) and broader study team, facilitating risk-focused discussions and driving clear, practical mitigation strategies.

This role can be based anywhere in the UK.

Key Responsibilities

  • Lead and maintain study-level risk assessments for assigned sponsor studies
  • Facilitate and chair cross-functional risk review meetings, ensuring focus on critical data and processes
  • Drive proactive identification, discussion, and documentation of study risks
  • Partner closely with the CRM and study team to ensure aligned oversight and follow-through on mitigation actions
  • Review centralized monitoring outputs, KRIs, KPIs, and trends to detect emerging or systemic risks
  • Support issue escalation, root cause analysis, and risk mitigation planning
  • Ensure risk-based activities align with set principles and sponsor expectations
  • Contribute to inspection readiness through clear documentation and defensible oversight decisions

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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What You Bring

  • Experience in clinical trial operations, study management, monitoring, or centralized oversight
  • Solid understanding of risk-based monitoring and study management principles
  • Knowledge of ICH-GCP, regulatory standards, and quality frameworks
  • Strong facilitation skills with confidence leading cross-functional discussions
  • Analytical mindset with the ability to interpret data, trends and signals
  • Excellent communication and stakeholder management skills
  • Ability to operate independently while collaborating effectively with sponsor and ICON team

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

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Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.

If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

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Skills

Risk-Based Study Management
Clinical Trial Operations
Centralized Monitoring
ICH-GCP
Stakeholder Management
Root Cause Analysis
Risk Assessment
Facilitation
Data Interpretation
Regulatory Standards
Quality Frameworks
Clinical Research Management

Location

Northern Ireland, United Kingdom

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