Senior CRA

ICON plc

. Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards .

Posted 11/9/2026full-timeRemote • DenmarkSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial activities, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) standards. Proficient in site management, data integrity, and effective stakeholder communication.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceGood Clinical Practice (GCP)Site MonitoringData Integrity

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesSite ManagementData CollectionProblem-SolvingProject Management

Soft Skills

Communication SkillsInterpersonal SkillsStakeholder ManagementOrganizational Skills

Tools & Technologies

Clinical Trial Software

Industry Keywords

Life SciencesNursingMedicineClinical Research AssociateParticipant Safety

About the role

Key responsibilities & impact

Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conduct site visits to assess site performance, resolve issues, and provide support for successful trial execution
Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
Provide training and guidance to site staff and other CRAs
Build and maintain effective relationships with site personnel and stakeholders
Ensure data integrity, participant safety, and compliance throughout the study lifecycle

Requirements

What you’ll need

Advanced degree in a relevant field such as life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
Ability to travel at least 60% of the time (international and domestic - fly and drive)
Valid driver’s license
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