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Clinical Research Associate
ExcelyaClinical Research Associate at Excelya, monitoring international clinical trials and ensuring protocol adherence. Contributing to clinical operations in a dynamic, ambitious team environment in Greece.
Tech Stack
Tools & technologiesGoogle 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 resumeApplicant 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