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Salary
$32k – $48k per year
Location
In office (Athens)
Seniority
Staff
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 4, 2026. First seen by Alion on Nov 2, 2026. IQVIA scores B on the Alion truth index.

Overview
Company
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Profile match
IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward.

Quality Lead, Computer System Validation & Regulatory Compliance

We are seeking an experienced Quality Lead to provide quality assurance leadership and

regulatory compliance oversight for business-critical technology solutions. This role serves as

the primary liaison between Quality Management and project teams, ensuring that computer

systems are developed, validated, and maintained in accordance with applicable regulatory

requirements and internal quality standards.

The successful candidate will play a key role in guiding teams through the Software

Development Life Cycle (SDLC), ensuring compliance with regulations and industry best

practices for computerized systems validation (CSV). This position combines quality leadership,

risk management, process improvement, and hands-on collaboration with product,

engineering, testing, and business teams.

Key Responsibilities

Regulatory Compliance & Quality Oversight

  • Provide expert guidance on quality assurance and regulatory compliance requirements

throughout the system development lifecycle.

  • Ensure computerized systems are validated and maintained in compliance with

applicable regulations, industry standards, and IQVIA quality processes.

  • Review and approve SDLC deliverables, validation documentation, and quality records.
  • Support project teams in interpreting and applying regulatory requirements to

technology solutions and business processes.

  • Identify compliance gaps, deviations, and quality risks, ensuring appropriate escalation

and resolution.

Computer System Validation (CSV)

  • Lead quality oversight activities related to system validation, testing, releases, and data

migration efforts.

  • Review validation documentation including requirements, risk assessments, test plans,

test cases, test evidence, and validation reports.

  • Ensure releases are appropriately classified (Operational, Patch, Minor, or Major) in

accordance with SDLC guidelines.

**PLEASE SUBMIT YOUR CV IN ENGLISH!

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

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.

The potential base pay range for this role, when annualized, is €28,500.00 - €42,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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