I

Icon

Global drug and device development services

Lead Business Operations Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • Comprehensive clinical research experience collaborating with global teams in a matrixed organizational environment.
  • Significant clinical research experience in one or more of the following areas: Risk-Based Quality Management (RBQM), Clinical Operations, Central Monitoring, Clinical Risk Management, or Clinical Data Science.
  • Strong knowledge of ICH E6 (R2/R3), ICH E8, and their application to RBQM.
  • Deep understanding of clinical trial processes, data flows, and risk-based monitoring strategies.
  • Demonstrated expertise implementing RBQM methodologies for multiple projects.
  • Ability to lead cross-functional initiatives and influence stakeholders globally.
  • Ability to translate regulatory expectations into operational practice.
  • Ability to operate effectively in complex, global environments.
  • Strong critical thinking and risk anticipation capabilities.

Responsibilities

  • Lead execution of Quality and Risk Management planning in alignment with study and program objectives.
  • Facilitate cross-functional workshops to identify and document Critical-to-Quality (CtQ) factors, critical data, and critical processes.
  • Coordinate and oversee initial and ongoing risk assessments, ensuring timely identification of risks and implementation of mitigation strategies.
  • Ensure risk assessments, risk controls, and mitigation plans are complete, actionable, and aligned with regulatory expectations.
  • Partner with Clinical Operations, Data Management, Biostatistics, and other stakeholders to review data flows, critical data pathways, and data review requirements.
  • Provide input into Risk-Based Monitoring (RBM) strategies, including targeted source data verification/source data review (SDV/SDR) approaches and reduced verification models.
  • Perform quality gate reviews of functional plans to confirm integration of risk mitigation and monitoring strategies.
  • Lead and facilitate Risk Review Meetings (RRMs) and ensure comprehensive documentation of risk evaluations and decisions.
  • Oversee ongoing risk surveillance to ensure monitoring strategies remain effective and aligned with study timelines and budgets.
  • Ensure risk review outputs provide meaningful insights, trend analysis, and actionable recommendations.
  • Update risk assessments based on protocol amendments, emerging signals, or changes to critical data and processes.
  • Support program-level and organizational RBQM governance and oversight activities.
  • Contribute to continuous improvement initiatives to enhance RBQM maturity and effectiveness across the organization.

Desired Qualifications

  • Proactive, solutions-oriented approach with a strong focus on quality and continuous improvement.
  • Strong communication, stakeholder engagement, and facilitation skills.
  • Passion for mentoring teams and strengthening RBQM capabilities across the organization.
  • Commitment to fostering an inclusive and collaborative culture.

About the Company

Icon

Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

Recently Posted Jobs

Explore more opportunities at Icon

See more jobs