Clinical Study Manager

ICON plc

. Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines .

Posted 10/7/2026full-timeRemote • Pennsylvania • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial management, ensuring compliance with regulatory requirements and maintaining data integrity throughout the study lifecycle. Proven ability to lead cross-functional collaboration and manage project timelines and budgets effectively.

Highest-signal resume keywords

Clinical Study ManagementRegulatory ComplianceProject ManagementData IntegrityCross-Functional Collaboration

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ManagementBudget ManagementResource AllocationStudy Timeline ManagementData Validation Processes

Soft Skills

Strong CommunicationInterpersonal SkillsDetail-OrientedProblem ResolutionCollaboration

Industry Keywords

Drug Development ProcessClinical TrialsRegulatory RequirementsStudy PlansQuality Standards

About the role

Key responsibilities & impact

Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines
Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies
Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans
Lead the resolution of issues and challenges that may arise during clinical trials
Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle
Coordinate clinical trial management delivery, resolve issues, and develop team capability

Requirements

What you’ll need

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements
Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively
Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners
Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials
Legal right to work in the country where the role is based

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