Clinical Trial Associate

ICON plc

. Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements .

Posted 9/17/2026full-timeRemote • HungaryJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in clinical trial coordination and administration, ensuring compliance with protocols and regulatory requirements while effectively managing documentation and communication across teams.

Highest-signal resume keywords

Clinical Trial CoordinationRegulatory ComplianceClinical Research ExperienceOrganizational SkillsCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills

Clinical Trial ProcessesData InterpretationStudy DesignRegulatory SubmissionsMetrics Tracking

Soft Skills

Attention to DetailCollaborationFast-Paced Environment Adaptability

Industry Keywords

Informed Consent FormsCase Report FormsClinical Trial DocumentationHealthcare-Related FieldScientific Degree

About the role

Key responsibilities & impact

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements
Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions
Support the preparation of study-related materials, such as informed consent forms and case report forms
Work with cross-functional teams to facilitate communication and ensure smooth trial execution
Contribute to the tracking and reporting of clinical trial metrics and milestones
Assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies

Requirements

What you’ll need

Bachelor's degree in a scientific or healthcare-related field
Prior experience or strong interest in clinical research
Knowledge of clinical trial processes, regulations, and guidelines
Excellent organizational and communication skills
Ability to work collaboratively in a fast-paced environment with attention to detail
Willingness to travel as required (approximately 10%)
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