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Data Quality Analyst

Job in Quality, Kern County, California, USA
Listing for: Clinical ink
Full Time position
Listed on 2026-01-14
Job specializations:
  • IT/Tech
    Data Analyst, Data Security
Job Description & How to Apply Below
Location: Quality

We're on a Mission to Advance Clinical Discovery

Patients are our ultimate why, and pioneering technology for patient outcomes is our DNA.

Join us to advance the life sciences industry with technology solutions that transform the clinical trial experience for patients and put our research clients on the path to making confident, better-informed decisions, faster.

When you join the Clinical ink team, you enjoy:

  • Robust benefits (medical, dental, vision, financial)
  • Unlimited vacation
  • Education assistance
  • Parental leave

Position:Data Quality Analyst

Location: Remote

Job :614

# of Openings:1

Company Information

Clinical ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in Philadelphia, PA, Winston Salem, NC, and Iowa City, IA, Clinical ink is rewriting the clinical development experience.

Job Description

Clinical ink is seeking a Data Quality Analyst to join our Data Quality team based remotely across the United States! This individual will contribute to verifying and validating data reports and exports for clinical trial software. The Data Quality Analyst’s responsibilities include:

  • Develop and oversee execution of testing strategies to validate data reports, exports and end of study deliverables
  • Ensure report requirements and data transfer specifications are clear, testable, and consistent with the clinical trial protocol
  • Perform accurate data entry with a focus on generating both positive and negative test cases to ensure comprehensive coverage of system validation scenarios
  • Proofread requirements for spelling and congruency with clinical trial protocol
  • Document testing in accordance with applicable process and procedures
  • Document and track defects to resolution
  • Perform other related duties as assigned/needed
Qualifications
  • Associate’s degree or equivalent experience
  • Proficiency with Microsoft Excel
  • Basic SQL knowledge
  • Experience with Salesforce, SAS, and Python is a plus but not required
  • Detail oriented and analytical reasoning skills
  • Strong written/verbal communication skills; ability to communicate with personnel at various levels
  • Effective prioritization, time management, and organizational skills
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