hirly

ICON

Clinical Data Coordinator

Poland, Warsaw

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at ICON first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.5M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Mid level
Country
PL
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

  • Clinical Trial Data Coordinator I ( CDC) / Junior Clinical Data Manager (CDM) / Clinical Data Reviewer / junior Clinical Trial Data Manager - Hybrid - Warsaw, Poland
  • ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Clinical Data Coordinator to join our diverse and dynamic team.

In this role you will be responsible for the review and verification of extensive clinical trial datasets, the identification of discrepancies or incomplete records, and the creation and resolution of queries to ensure data accuracy and consistency.

What you will be doing :

Review clinical trial data captured in electronic data capture systems

Identify missing, inconsistent, or out-of-range data

Generate, track, and resolve data queries

Ensure data aligns with study protocols and data management plans.

Perform ongoing data quality checks and trend reviews.

Your profile :

Master’s degree in a relevant field (e.g., Life Sciences or Healthcare, Biology, Pharmacy, etc), candidates in the final stage of their Master’s studies can also be considered.

Availability to commence work on 2nd November

Able to work in a hybrid setup: 3 days per week on-site at the client’s office in Warsaw

Fluent English

Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry.

Familiarity with data management software and systems

Strong attention to detail and the ability to work effectively in a fast-paced environment.

Excellent communication skills and the ability to collaborate with cross-functional teams.

#LI-DS1

#LI-Hybrid

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .

Are you a current ICON Employee? Please click here to apply

Original posting on ICON's site ↗

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job