1d ago
New

Site Study Coordinator

GreeceGreece·ThessaloníkiFull-timemid
Research AssociateLaboratory & Life Sciences
0 views0 saves0 applied

Quick Summary

Key Responsibilities

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.

Requirements Summary

Responsible for maintaining Investigator Site Files (ISF) and ensure documents are accurate, complete, and inspection/audit-ready.

Technical Tools
Research AssociateLaboratory & Life Sciences

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 Role

~1 min read

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.

    • 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

~1 min read

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.

 

What We Offer

~1 min read
✓Car/car allowance
✓Fuel expenses
✓On-site visit expenses
✓Mobile phone
✓Laptop
✓Private health insurance

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!

Location & Eligibility

Where is the job
Thessaloníki, Greece
On-site at the office

About this job

Posted
1 day ago
Employer
has 44 open jobs on Jobera in 8 countries.

Listing Details

Posted
October 27, 2026
First seen
October 27, 2026
Last seen
October 28, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
67%
Scored at
October 28, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions.

Employees
501-1,000
View company profile
Newsletter

Stay ahead of the market

Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.

A
B
C
D
Join 12,000+ marketers

No spam. Unsubscribe at any time.

Site Study Coordinator