Experienced Clinical Research Associate - CZ Republic

QHR IQVIA Zagreb d.o.o.

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Prague, Czech Republic Until 8/21/2026 First posted April 20, 2026 Last posted April 20, 2026
Job description

Clinical Research Associate

Your responsibilities will include:

  • Performing site selection, initiation, monitoring and close-out visits

  • Supporting the development of a subject recruitment plan

  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines

  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions

  • Collaborating with experts at study sites and with client representatives


Qualifications:

  • University degree in scientific discipline or health care

  • At least 2 year of experience as a Clinical Research Associate.

  • Very good computer skills including MS Office

  • Excellent command of Czech and English language. CZ Republic based.

  • Organizational, time management and problem-solving skills

  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients

  • Flexibility to travel

  • Driver’s license class B

What you can expect:

  • Resources that promote your career growth

  • Leaders that support flexible work schedules

  • Programs to help you build your therapeutic knowledge

  • Excellent working environment in a stabile, international, reputable company

  • Company car, mobile phone and attractive benefits package

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.

About this role

Summary

Manage site activities, ensure compliance, support recruitment, and collaborate with study teams in clinical research.

Job title

Experienced Clinical Research Associate - CZ Republic

Experience level

2+ years

Industry

healthcare

Location requirements

Prague, Czech Republic; on-site with travel flexibility

Salary

Not specified

Management role

No

Skills & keywords

Required skills

university degreeclinical research experienceMS Officelanguage skills Czech, Englishdriver’s license

Preferred skills

clinical trialsregulatory knowledgetravel flexibility

Specializations

clinical researchregulatory compliancesite management
Locations

Structured locations inferred from the posting.

Prague, Czechia

On-site City