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Analyst - Computer Software Validation

Veeva Systems

remote,Croatia - ZagrebDataFull-time
Salary30000EUR-50000EUR
Before you apply

Role details

The practical picture
Employment
Full-time
Role signal brief

The role, at a glance

Extracted from the source posting · 95% confidence

Veeva Systems seeks a Computer Software Validation specialist for their Randomization and Trial Supply Management (RTSM) team, requiring 1+ year of CSV experience in clinical trial software and knowledge of regulations such as 21 CFR Part 11. The remote role with Work Anywhere policy allows working from home or office, supporting customer RTSM implementations in a fast-paced environment.

Compensation
EUR 30,000–50,000 / year

What you need

  • 1+ year of experience in computer software validation for clinical trial software (CTMS, CDMS, eTMF, etc.)
  • Working knowledge of software development cycle (SDLC)
  • Working knowledge of GCP Guidance such as 21 CFR Part 11, EU Annex 11
  • Exceptional attention to detail
  • Good interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levels

What you will own

  • Participate in RTSM requirement gathering sessions with clients and team members
  • Collaborate with Development and Project Management teams to define clear, testable, compliant requirements
  • Ensure requirements are adequately tested following a risk-based approach
  • Develop and maintain CSV deliverables including requirements specifications, test scripts, summary reports, and trace matrices
  • Manage validation testing cycles and resolve issues/enhancement requests
  • Maintain change control documentation for ongoing RTSM system validation
Core skills
Computer System ValidationClinical Trial SoftwareRequirements GatheringTest Script Development21 CFR Part 11GAMP5Risk-Based TestingTraceability MatrixMicrosoft WordMicrosoft Excel

Remote policyWork Anywhere policy, allowing you to work in an office or at home on any given day

Internal freshness window ends Oct 21, 2026
View source evidence
  • title “Analyst - Computer Software Validation”
  • company “Veeva Systems”
  • location “remote,Croatia - Zagreb”
  • remote_scope “This is a remote role with Veeva's Work Anywhere policy, allowing you to work in an office or at home on any given day”
  • applicant_location_requirements “None specified beyond remote work”
  • timezone_requirements “Not specified”
  • must_have “1+ year of experience in a CSV for clinical trial software”
  • must_have “Working knowledge of GCP Guidance such as 21 CFR Part 11, EU Annex 11”
  • nice_to_have “Familiarity with the conduct of clinical trials”
  • nice_to_have “Previous experience with RTSM”
  • company_remote_policy “As a Work Anywhere company, we support your flexibility to work from home or in the office”
  • salary “Total compensation: 30,000 - 50,000 EUR”
computer system validationclinical trial softwarerequirements gatheringtest script development
Role brief
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.   At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.   As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.   Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

We are looking for a Computer Software Validation (CSV) professional with a specialty in clinical trial software. This role would give you the opportunity to work on a leading solution in Randomization and Trial Supply Management (RTSM) software. To excel in this role, you will require strong technical writing capabilities and the ability to simplify complex topics.   As a member of the RTSM team, you will work closely with Development and Project Management teams to support customer RTSM implementations in a fast-paced environment. You will use your expertise to take ownership of the validation process for assigned projects and play an important role in building and maintaining product excellence for the RTSM system.   This is a remote role with Veeva’s Work Anywhere policy, allowing you to work in an office or at home on any given day. It’s about getting the work done in the way and place that works best for each person.

What You'll Do

  • Participate in RTSM requirement gathering sessions with clients and RTSM team members
  • Closely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear, testable, and compliant format
  • Ensure requirements are adequately tested following a risk-based approach
  • Develop and maintain CSV deliverables including requirements specifications, test scripts, summary reports, and trace matrices
  • Manage Validation testing cycles and resolution of issues and enhancement requests
  • Maintain change control documentation to ensure ongoing validation of the RTSM system
  • Provide technical expertise to RTSM team members in computer system validation, applicable regulations, and other quality system requirements
  • Support customers as needed in RTSM validation activities

    • Requirements

  • 1+ year of experience in a CSV for clinical trial software (CTMS, CDMS, eTMF, etc.)
  • Working knowledge of software development cycle (SDLC)
  • Working knowledge of GCP Guidance such as 21 CFR Part 11, EU Annex 11
  • Exceptional attention to detail
  • Good interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levels

    • Nice to Have

  • Familiarity with the conduct of clinical trials
  • Previous experience with RTSM
  • Expert in Microsoft Word and Excel

    • Interviewing with Veeva

    We value your time and believe in a transparent hiring process. Here is the process you can expect.
  • Follow the application process and submit your resume.
  • Within 3 days, you will receive a link to a personality assessment administered by a third party.
  • Once you complete the assessment, our team will review your full application package and follow up via email with our decision.
  • If moving to the interview stage, the process is as follows:
    1. A conversation with the hiring manager
    2. A practical case exercise
    3. A final conversation with our group's Senior Leader.
  • Once all interviews are complete, the manager will be in touch with a final decision. 

    • Compensation

  • Total compensation: 30,000 - 50,000 EUR
  • The total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Please note that actual total compensation may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position's total compensation may be composed of other types of compensation, such as variable bonus and/or stock bonus.

    • Additional

    #RemoteCroatia #LI-Associate
    Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.   As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.   If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@veeva.com.