IQVIA is hiring Clinical Research Associate (CRA) 1/2 for a Sponsor Dedicated role in Bratislava, Slovakia. This is an excellent opportunity for professionals seeking clinical research jobs, CRA careers, and growth in the global pharmaceutical and clinical trials industry.
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About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company creates intelligent connections to accelerate the development and commercialization of innovative medical treatments, helping improve patient outcomes and population health worldwide.
With a strong reputation for innovation, regulatory compliance, and operational excellence, IQVIA offers professionals the chance to work on cutting-edge clinical trials in a dynamic, global environment.
Job Details
- Company Name: IQVIA
- Experience: Entry-level to mid-level (training provided)
- Qualification: Bachelor’s Degree (scientific discipline or healthcare preferred)
- Location: Bratislava, Slovakia
- Work Type: Full-time, On-site
Job Description
IQVIA is offering a structured training program for Clinical Research Associates to develop the skills needed to independently conduct clinical monitoring visits. This Sponsor Dedicated role focuses on ensuring high-quality execution of clinical trials in compliance with protocols, GCP, and regulatory requirements.
Clinical Research Associate 1/2 – Sponsor Dedicated
- Department: Clinical Monitoring / Clinical Operations
- Role: Clinical Research Associate
- Experience: Entry to mid-level
- Education/Qualification: Bachelor’s Degree in scientific discipline or healthcare preferred
Skills/Qualifications
- Bachelor’s degree in a scientific or healthcare field
- General understanding of clinical trials and CRA responsibilities
- Excellent written and verbal communication skills in English and Slovak
- Strong organizational, problem-solving, and time management skills
- Knowledge of GCP, ICH guidelines, and applicable regulatory requirements
- IT literate with valid driver’s license
- Ability to build effective working relationships
Key Responsibilities
- Complete therapeutic, protocol, and clinical research training
- Perform site monitoring visits under supervision
- Administer protocol training and maintain site communication
- Evaluate site practices and escalate quality issues
- Track study progress including recruitment and data queries
- Manage Trial Master File and Investigator Site File documentation
- Prepare monitoring visit reports and follow-up letters
- Support study start-up and subject recruitment activities
Benefits/Perks
- Structured training and professional development program
- Opportunity to work on global clinical trials
- Exposure to sponsor-dedicated projects
- Collaborative and supportive work culture
- Long-term career growth in clinical research
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the IQVIA career page.
🔗 Click below to apply directly for this job
Interested candidates can apply directly through the official IQVIA careers portal. Visit: https://jobs.iqvia.com and search for requisition ID R1491633.
For more clinical research and pharma jobs worldwide, visit Pharma Recruiter.
Why You Should Join
IQVIA offers a dynamic, integrity-driven culture with a strong focus on innovation and employee development. As a global leader in clinical research, the company provides long-term career stability, continuous learning opportunities, and exposure to advanced clinical trials. Join IQVIA to build a rewarding career while contributing to the development of life-changing medical treatments.
FAQs
Q1: What qualifications are required for the CRA position?
A Bachelor’s Degree in a scientific discipline or healthcare is preferred. Prior clinical experience is advantageous but not mandatory.
Q2: Is this an entry-level role?
Yes. The position includes a structured training program suitable for candidates beginning their CRA career.
Q3: What languages are required?
Excellent command of both English and Slovak (written and verbal) is essential.
Q4: Where is the job located?
The role is based in Bratislava, Slovakia.