Clinical Research Associate

ICON plc

. Coordinate all activities for setting up and monitoring a study .

Posted 11/9/2026full-timeRemote • GermanyJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating clinical studies, ensuring compliance with regulatory requirements, and maintaining high standards in clinical trial monitoring. Proficient in developing collaborative relationships with stakeholders and analyzing laboratory results.

Highest-signal resume keywords

Clinical Trial MonitoringStudy Documentation ManagementRegulatory ComplianceLaboratory AnalysisBilingual Communication (English and German)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study CoordinationClinical Trial MonitoringLaboratory AnalysisStudy Documentation ManagementFeasibility Study Preparation

Soft Skills

Excellent CommunicationGood Social SkillsCollaboration

Industry Keywords

Medical DevicesPatient SafetyRegulatory RequirementsClinical InvestigatorsStakeholder Engagement

About the role

Key responsibilities & impact

Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Run sponsor generated queries efficiently and take responsibility for study cost efficiency
Participate in the preparation and review of study documentation and feasibility studies for new proposals as required
Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff
Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements
Deliver clinical trial monitoring work to a high standard across clinical programmes

Requirements

What you’ll need

University degree in medicine, science, or equivalent
Excellent written and verbal communication in English and German
Lab experience and / or ability to analyse laboratory results
Experience or interest in medical devices
Good social skills enabling you to deal with queries in a timely manner
Willingness to travel as required (approximately 60%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based

Benefits

Comp & perks

Stability, career development and a collaborative environment
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
Reasonable accommodations during the recruitment process