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Iqvia

Freelance CRA - Czech Republic

Prague, Czech Republic

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hirly's read of this role

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

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

the posting

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!

#LI-DNP

#LI-CES

#LI-HCPN

#LI-NS1

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.

Original posting on Iqvia's site ↗

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