Senior Clinical Research Associate

ICON plc

Senior Clinical Research Associate managing clinical trials to ensure compliance with protocols. Contributing to patient safety and data integrity in a global healthcare organization.

Posted 7/10/2026full-timeRemote • 🇫🇷 FranceSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Trial Monitoring, ensuring adherence to protocols and regulatory requirements while managing multiple sites effectively. Strong communication and stakeholder management skills facilitate collaboration and compliance in complex environments.

Highest-signal resume keywords

Clinical Trial MonitoringRegulatory RequirementsSite ManagementData IntegrityStakeholder Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesGood Clinical Practice (GCP)Site Performance AssessmentProblem-SolvingOrganizational Skills

Soft Skills

Communication SkillsInterpersonal SkillsInfluencing Skills

Tools & Technologies

Clinical Trial Software

Industry Keywords

Clinical Research AssociateLife SciencesNursingMedicine

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

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) and should possess a valid driver’s license

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