Live opening · Posted 6 hours ago

Site Study Coordinator

Excelya · Thessaloniki, Central Macedonia, Greece
Workable No
JobBeeper subscribers received an alert for this role.

At a glance

The key details from the original listing.

Posted 6 hours ago
CompanyExcelya
LocationThessaloniki, Central Macedonia, Greece
Work modeNo
SkillsGCP, Excel, Clinical Research, Data Entry, Documentation
SourceWorkable
ListedPosted 6 hours ago

About the role

Description supplied by the original job listing.

Redefine Clinical Operations. Empower Innovation. Build with Audacity.
Join Excelya as Our Next Clinical Star!
At Excelya, we don’t just work, we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of healthcare with one bold ambition: to become Europe's leading mid-size CRO, offering the best employee experience.
Now, we’re calling on curious minds and courageous spirits to step into a career-defining role in Clinical Operations. Ready to make an impact that travels the globe? Let’s talk.
About the Job
We are seeking a Study Coordinator to work at assigned hospitals to support Investigators and site staff with daily clinical trial activities. The Study Coordinator ensures smooth study conduct by coordinating operational tasks, supporting recruitment and data quality, and acting as an extended resource for the site. This role works closely with Investigators, nurses, other site staff and the Sponsor’s Clinical Operations team to maintain compliance with study protocols, GCP/ICH guidelines, and all applicable regulatory requirements. Traveling is part of the role.
Your Mission:
Responsible for maintaining Investigator Site Files (ISF) and ensure documents are accurate, complete, and inspection/audit-ready.
Support data entry and query (non-medical) resolution in EDC systems as delegated by the Principal Investigator.
Assist in adverse event (AE/SAE) reporting and follow-up.
Collection and shipment of biological samples including labelling and packaging.
IP accountability tasks as delegated by pharmacist or PI. Temperature monitoring of all IPs.
Assist with submissions or updates to Ethics Committees or hospital administration.
Requirements
What You Bring to the Table:
We are looking for candidates who embody our values of Audacity, Care, and Energy and also:
Degree in Life Sciences, Nursing, Pharmacy or related field.
Previous experience in clinical research (Study Coordinator or similar role preferred).
Knowledge of GCP and clinical trial processes.
Experience with EDC systems and clinical documentation.
Strong organizational and communication skills.
Ability to manage multiple tasks and coordinate across different sites.
Fluency in Greek and English.
Benefits
Benefits:
Car/car allowance
Fuel expenses
On-site visit expenses
Mobile phone
Laptop
Private health insurance
Why Choose Excelya?
At Excelya, we lead with Audacity, act with Care, and move with Energy. We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job, you’re becoming a key part of something bigger.
So, if you're ready to excel with purpose, let’s write the next chapter together!

Work arrangement
No

Your early-applicant advantage

Live timing from JobBeeper.

Live data
12 min median time from a role going live to a subscriber being told
6 hours subscribers had this role before this page existed
71,135 roles found in the last 24 hours — the newest are not on this site yet
See available plans →

More openings worth a look

Recently tracked roles with full details and direct application links.

6 roles
Good roles move before most people even see them. Tell JobBeeper what you want and get fresh matches delivered in minutes.
Create free account →
⚡ Get fresh job alerts 📱 Get App