Senior Clinical Trial Associate

ICON plc

Senior Clinical Trial Associate managing administrative tasks for clinical trials at ICON. Collaborating with teams and ensuring compliance throughout the trial process.

Posted 7/9/2026full-timeRemote • 🇹🇷 TurkeySeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial support, including regulatory compliance, documentation management, and effective communication with cross-functional teams. Proven ability to manage multiple projects and maintain strong relationships with stakeholders to ensure successful trial operations.

Highest-signal resume keywords

Clinical Trial Support ExperienceRegulatory ComplianceClinical Trial Management SystemsStrong Organizational SkillsExcellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesDocumentation ManagementData ManagementMultitaskingProblem-Solving

Soft Skills

Interpersonal SkillsCollaboration

Tools & Technologies

Clinical Trial Management Systems

Industry Keywords

Regulatory DocumentsStudy ProtocolsTrial OperationsSite CommunicationsStakeholder Relationships

About the role

Key responsibilities & impact

Provide administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records
Assist in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements
Collaborate with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study
Monitor and track trial progress, including managing site communications and ensuring timely delivery of study materials
Build and maintain strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success

Requirements

What you’ll need

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements
Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively
Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management
Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders
Willingness to travel as required (approximately 10%)

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