Asset Quality Lead

ICON plc

Asset Quality Lead ensuring quality compliance of clinical trials at ICON, a global healthcare intelligence organization. Leading quality assurance strategies and processes to support clinical trial activities.

Posted 7/7/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive expertise in quality assurance strategies and regulatory compliance within the pharmaceutical and biotechnology sectors, with a strong focus on leadership and cross-functional collaboration to enhance quality management systems.

Highest-signal resume keywords

Quality Assurance LeadershipRegulatory Compliance (ICH-GCP, FDA)Quality Management Systems ImprovementAnalytical Problem-SolvingCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Quality Assurance StrategiesQuality AssessmentsAuditsRegulatory RequirementsClinical Trials ComplianceCorrective Actions ImplementationQuality Management Documentation

Soft Skills

Communication SkillsInterpersonal SkillsCollaboration Skills

Industry Keywords

Pharmaceutical IndustryBiotechnology IndustryCRO IndustryLife SciencesPharmacy

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Leading the development and implementation of quality assurance strategies and processes to support clinical trial activities
Conducting comprehensive quality assessments and audits to ensure compliance with regulatory standards and guidelines
Collaborating with cross-functional teams to identify and address quality issues and implement corrective actions as needed
Providing expert guidance and support to staff regarding quality assurance policies, procedures, and best practices
Contributing to the continuous improvement of quality management systems and documentation

Requirements

What you’ll need

Bachelor's degree in Life Sciences, Pharmacy, or related field; advanced degree preferred
Minimum of 10 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry, with significant experience in a leadership role
Extensive knowledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations)
Strong analytical and problem-solving skills, with the ability to identify and resolve complex quality issues
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders
Willingness to travel as required (approximately 25%)

Benefits

Comp & perks

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