Live opening · Posted 7 days ago

Freelance CRA - Czech Republic

IQVIA · Prague, Czech Republic
Workday
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At a glance

The key details from the original listing.

Posted 7 days ago
CompanyIQVIA
LocationPrague, Czech Republic
SourceWorkday
Listed7 days ago

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About the role

Description supplied by the original job listing.

Join IQVIA Biotech as a Freelance Clinical Research Associate supporting two Phase III Oncology clinical trials. You’ll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team.
Location: Czech Republic, travel required (sites are located in Brno, Prague, Ostrava, Hradec Kralove)
FTE: 0.5
Start: ASAP
Duration: around 5 months, potential for extension
Your Role
Conduct site evaluations, initiations, monitoring & close-outs
Ensure GCP compliance and data integrity
Collaborate with investigators and internal teams
Review protocols, study manuals, and eCRFs
Support site staff with training and issue resolution
Track investigational product inventory and documentation
Attend investigator meetings and study-related events
Contribute to audit readiness and inspection support
Your Profile:
2+ years CRA including site monitoring experience
Oncology/Hematology experience
Strong knowledge of clinical trial processes & GCP
Excellent communication & organizational skills
Ability to work independently and manage priorities
Fluent in Czech and English
If you're ready to make an impact in clinical research, apply today!
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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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