Clinical ink logo
Clinical ink
Posted 77 days agoVerified live 5h ago

Validation Analyst

Brief overview

Remote
UndergradOr in progress
8 H-1B approvalsDept. of Labor
1 green cardsCertified filings
Test script developmentClinical trial software testingRequirement analysis for clinical trialsProtocol-specific testingQualification testingDefect documentation and trackingData report validationMicrosoft WordMicrosoft ExcelAnalytical reasoning

About the company

Clinical ink logo
Clinical inkclinicalink.com

Clinical Ink develops electronic documents recording software for recording source data on mobile devices during clinical trials.

Visa sponsorship history

3 years sponsoring, last filed FY2026

Data powered by U.S. Department of Labor. This does not guarantee sponsorship for this specific role.
8H-1B approved
100%approval rate
5new H-1B hires
1PERM certified
$197,500median wage / yr
H-1B Petition ApprovalsVisas USCIS actually granted: the strongest sign the company sponsors.
20242
20255
20261
LCA Certified ApplicationsAn early filing step, not a visa approval: it signals intent, not confirmed sponsorship.
20252
Green Card (PERM) FilingsCertified green card filings: a long-term commitment to international hires.
20261
Top sponsored roles
Principal Quality EngineerVP, Business Development

Job description

Summary

Clinical Ink is a global life science company that brings data, technology, and patient science together to unlock clinical discovery. They are seeking a Validation Analyst to develop and oversee the execution of test scripts for clinical trial software, ensuring the software functions correctly and maintains the integrity of clinical study data.

Responsibilities

  • Develop and oversee the execution of testing scripts
  • Ensure the correct functioning of clinical trial software with focus on patient safety and integrity of clinical study data by: Ensuring requirements are clear, testable, and consistent with the clinical trial protocol
  • Proofreading requirements for spelling and congruency with clinical trial protocol
  • Scripting and/or conducting protocol/project specific testing to ensure fulfillment of study design, build, and implementation requirements
  • Documenting testing in accordance with applicable process and procedures
  • Executing qualification testing on section build requirements
  • Executing qualification testing on form design requirements
  • Documenting defects and tracking to resolution
  • Verifying approved study-specific configuration settings
  • As required, assist with the execution of platform testing
  • Provide cross-functional support to Data Quality, as needed, including: Verify and validate data reports and exports, Verify data clarifications
  • Perform other related duties as assigned

Skills

  • Associates degree or relevant experience
  • Strong written/verbal communication skills; ability to communicate with personnel at various levels
  • Exceptional computer skills; proficiency with Microsoft Word, Excel, etc
  • Detail-oriented and analytical reasoning skills
  • Sense of ownership and proactive approach to work
  • Effective prioritization, time management, and organizational skills

Qualifications

Must Haves

  • Associates degree or relevant experience
  • Strong written/verbal communication skills; ability to communicate with personnel at various levels
  • Exceptional computer skills; proficiency with Microsoft Word, Excel, etc
  • Detail-oriented and analytical reasoning skills
  • Sense of ownership and proactive approach to work
  • Effective prioritization, time management, and organizational skills

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