Excelya

Clinical Research Associate

Excelya

full-time

Posted on:

Location Type: Hybrid

Location: Paris • France

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Tech Stack

Google Cloud Platform

About the role

  • Conduct site initiation, monitoring, and close-out visits.
  • Ensure site compliance with study protocols, ICH-GCP guidelines, and applicable regulations.
  • Communicate effectively with study sites to facilitate trial conduct and resolve any issues.
  • Review and verify study-related documents and data to ensure accuracy and completeness.
  • Monitor patient safety and data integrity throughout the study.
  • Participate in preparation for audits and regulatory inspections.
  • Provide regular updates to project managers and stakeholders on site progress and any challenges.

Requirements

  • Minimum 2 years' experience as a Clinical Research Associate (CRA), ideally in oncology or similar therapeutic areas.
  • Good understanding of clinical trial processes and regulatory requirements.
  • Excellent interpersonal and communication skills, both written and verbal.
  • Bachelor's degree in life sciences, pharmacy, or a related field.
  • Master's degree or additional certification in clinical research is a plus.
  • Fluent in English.
Benefits
  • Why join us?
  • At Excelya, we combine a passion for science with a commitment to teamwork to redefine excellence in healthcare. Here’s what makes us unique.
  • We are an ambitious, fast-growing healthcare company of 900 Excelyates, with the goal of becoming the leading mid-sized CRO in Europe and providing the best employee experience. Our “one-stop provider” service model—offering full-service, functional service provider (FSP), and consulting—allows you to work across a variety of projects. By working alongside recognized experts, you will help advance scientific, operational, and human knowledge to enrich the patient journey.
  • “Excelling with care” means benefiting from an environment that values your natural talents, pushes boundaries with boldness, and supports your development, enabling you to contribute fully to our shared mission.
Applicant Tracking System Keywords

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

Hard Skills & Tools
clinical trial processesstudy protocolsICH-GCP guidelinesdata integrity monitoringaudit preparationregulatory inspections
Soft Skills
interpersonal skillscommunication skillsproblem-solvingteam collaboration
Certifications
Bachelor's degree in life sciencesBachelor's degree in pharmacyMaster's degree in clinical research