Clinical Research Associate – Investigator Site

Excelya

. Enter clinical data into electronic case report forms (eCRFs) .

Posted 9/25/2026full-timeParis • FranceJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data management, ensuring compliance with Good Clinical Practice (GCP) while effectively coordinating clinical research activities. Proficient in data entry and eCRF tools, with strong organizational skills and attention to detail to support the execution of clinical studies.

Highest-signal resume keywords

Clinical Trial Technician (CTT)Clinical Research Associate (CRA)Good Clinical Practice (GCP)Data Entry ProficiencyOncology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ManagementData EntryECRF ToolsSource Document ReviewOperational Follow-Up

Soft Skills

Organizational SkillsAttention to DetailTeam CollaborationPrioritization SkillsDeadline Management

Industry Keywords

Clinical ResearchGood Clinical Practice (GCP)Clinical StudiesInvestigator SitesMonitoring Visits

About the role

Key responsibilities & impact

Enter clinical data into electronic case report forms (eCRFs)
Manage and resolve queries with investigator sites and project teams
Review source documents to ensure data quality, consistency, and completeness
Prepare for and support monitoring visits by ensuring the availability and organization of the required documentation
Provide operational follow-up for investigator sites and contribute to the smooth execution of clinical studies
Travel regularly throughout France to support sites, assist local teams, and ensure the quality of collected data
Participate in coordinating clinical research activities with medical teams, investigators, and the various study stakeholders
Ensure compliance with Good Clinical Practice (GCP) and applicable procedures throughout the study

Requirements

What you’ll need

Degree or training in clinical research, life sciences, healthcare, or an equivalent field (2–5 years of post-secondary education)
Previous successful experience as a Clinical Trial Technician (CTT), Clinical Research Associate (CRA), or Clinical Research Assistant
Oncology experience is a plus
Proficiency in data entry and eCRF tools
Good knowledge of Good Clinical Practice (GCP)
Thoroughness, organizational skills, and attention to detail
Ability to work as part of a team and interact with a range of stakeholders
Strong prioritization skills and ability to meet deadlines
Ability to read and understand scientific English
Regular travel throughout France

Benefits

Comp & perks

Young and ambitious healthcare company with 900 employees
Integrated services model covering full-service solutions, functional services, and consulting
Opportunities for career development through varied projects
Collaboration with leading experts
An environment that recognizes natural talents, boldly pushes boundaries, and nurtures potential
Opportunity to contribute to a mission focused on improving the patient journey