Global Study Manager

ICON plc

Global Study Manager overseeing end-to-end delivery of oncology studies in a collaborative environment. Ensuring compliance with regulations and leading project teams across functions.

Posted 5/28/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesMid-LevelSeniorWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

clinical developmentstudy delivery strategyvendor managementrisk assessmentOncology clinical trialsoperational study deliveryclinical plansissue resolutionproject management

Soft Skills

leadershipinfluencingnegotiationcollaborationproblem-solvingrelationship buildingmatrix managementcommunication

Certifications & Qualifications

Bachelor’s degree in life sciences

Industry Keywords

ICH guidelinesGCP guidelinespharmaceutical industryCRO environmentstudy timelinesstudy qualitypatient engagementdiversity in studies

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead the global study delivery strategy (e.g., country selection, diversity, patient engagement strategy, recruitment plan, etc)
Drive assessment, selection, engagement, and management of appropriate vendors
Ensure compliance with ICH/GCP guidelines, all applicable laws and regulations, and client SOPs, for all products and services delivered for their designated studies
Make decisions which balance risk/benefit with clear understanding of impact on the study and project; takes action to mitigate risk where appropriate
Actively partner to build relationships and collaborate with oncology aligned staff in other global functions
Encourage others within matrix and line teams to seek alternative perspectives and develop solutions
Lead / support the conduct of investigator meetings and other study related meetings

Requirements

What you’ll need

Bachelor’s degree in life sciences or related discipline
Considerable clinical development experience that is equivalent to 3 years as a global study leader with proven experience in driving operational study delivery to time, cost, and quality within the pharmaceutical industry or CRO environment
Proven operational experience of leading high performing global study teams in Oncology clinical trials
Proactively identify and resolve issues to ensure timely study delivery to quality, timelines, and budget
Strong leadership, influencing and negotiation skills
Demonstrated experience leading in the matrix environment to deliver projects, develop clinical plans and manage change

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