Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Excelya

Clinical Research Associate

Excelya

Clinical Research Associate at Excelya, monitoring international clinical trials and ensuring protocol adherence. Contributing to clinical operations in a dynamic, ambitious team environment in Greece.

Posted 6/15/2026full-timeAthens • 🇬🇷 GreeceJuniorMid-LevelWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Join Excelya, where **Audacity, Care, and Energy** define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
  • This role is an exciting opportunity to contribute to a dynamic, ambitious team in **Clinical Operations**. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.
  • **Main Responsibilities:**
  • - Perform monitoring of international clinical trials across Phases I–IV, ensuring protocol adherence and data integrity at investigational sites.
  • - Guarantee scientific, regulatory, and technical quality through meticulous oversight and application of GCP and local regulatory standards.
  • - Manage investigational product (IP) logistics including reconciliation, storage, dispensing, and inventory, with special focus on blinded/randomized protocols.
  • Beyond that, you will also be able to:
  • - Review and reconcile Investigator Site Files (ISF) with the Trial Master File (TMF) and ensure proper document archiving as per regulatory requirements.
  • - Conduct routine monitoring and co-monitoring visits with CRAs to ensure source data verification, site performance, and resolution of deviations via CAPA processes.
  • - Draft comprehensive monitoring visit reports in English and support audit readiness across all clinical sites.

Requirements

What you’ll need
  • **About you:**
  • At Excelya, **taking audacious steps is encouraged**, so we’re looking for individuals who are ready to grow with us and share our values.
  • **Experience**: Minimum of 1 year of experience in monitoring activities as a CRA.
  • **Skills**: Good communication and organization skills, focus to detail, time management, multi-tasking, very good knowledge of PC, willingness to travel.
  • **Education**: Bachelor’s degree in life and/or health sciences is preferred - post graduate studies in a relative field are considered as a plus.
  • **Languages**: Fluency in English and Greek language.

Benefits

Comp & perks
  • **Why Join Us?**
  • At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
  • Here’s what makes us unique
  • We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s **leading mid-size CRO** with the **best employee experience**. Our **one-stop provider service model**, offering full-service, functional service provider, and consulting, enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.
  • **Excelling with care** means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
  • **Excelling with Care**
  • At Excelya, **Care **lies at the heart of what we do. We provide equal opportunities for all and foster a diverse, equitable, and inclusive workplace where humility and boldness work hand in hand. Everyone has a space to feel valued, thrive, and collaborate with purpose.
  • Your challenges become our shared mission. Together, we transform bold ideas into reality—the Excelya way.
  • **Apply today, become an Excelyate!**

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills & Tools
monitoring activitiesclinical trialsGCPregulatory standardsinvestigational product logisticsdocument archivingsource data verificationCAPA processesmonitoring visit reportsTrial Master File
Soft Skills
communication skillsorganization skillsattention to detailtime managementmulti-taskingcollaborationpersonal growthintellectual growthaudacitywillingness to travel