Clinical Trial Associate

ICON plc

. Conduct in-depth feasibility assessments for clinical trials, including evaluating site capabilities, resource availability, and potential risks .

Posted 11/10/2026full-timeRemote • ChinaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in conducting clinical trial feasibility assessments, analyzing data, and preparing comprehensive reports. Strong ability to build relationships with stakeholders and mentor junior team members while staying informed on industry trends and regulatory requirements.

Highest-signal resume keywords

Clinical Trial Feasibility AssessmentsData Analysis ToolsProject ManagementAnalytical SkillsCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ProcessesSite ManagementFeasibility ReportingData InterpretationResource Evaluation

Soft Skills

Interpersonal SkillsOrganizational SkillsMentorship

Industry Keywords

Regulatory RequirementsStakeholder EngagementContinuous ImprovementClinical Trial PlanningSite Performance Metrics

About the role

Key responsibilities & impact

Conduct in-depth feasibility assessments for clinical trials, including evaluating site capabilities, resource availability, and potential risks
Collaborate with clinical operations teams, project managers, and other stakeholders to gather and analyze data relevant to trial feasibility
Prepare comprehensive feasibility reports and recommendations to support project planning and decision-making processes
Analyze historical data and site performance metrics to identify trends, opportunities, and challenges impacting trial feasibility
Develop and maintain strong relationships with clinical sites, investigators, and external partners
Stay up-to-date with industry trends, regulatory requirements, and best practices related to clinical trial feasibility and planning
Provide mentorship and guidance to junior feasibility team members
Contribute to continuous improvement efforts within the team

Requirements

What you’ll need

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in clinical trial feasibility assessments, with a deep understanding of clinical research processes and site management
Exceptional analytical skills, with the ability to interpret complex data and provide actionable insights
Strong organizational and project management skills, with experience in handling multiple feasibility projects simultaneously
Excellent communication and interpersonal skills, with the ability to build and maintain effective relationships with stakeholders at all levels
Proficiency in data analysis tools and software relevant to feasibility assessments and clinical research
Willingness to travel as required (approximately 15%)
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