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Clinical Data Validation Jobs (NOW HIRING)

Everest Clinical Research Corporation

Establish and control clinical data operations to provide complete, valid, safe, and secure databases which meet corporate and regulatory clinical data requirements. Develop and manage clinical data ...

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Clinical Data Validation information

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$10

$39

$76

How much do clinical data validation jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical data validation in the United States is $39.26, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $51.92 per hour, depending on experience, location, and employer.

What is clinical data validation?

A Clinical Data Validation job involves verifying and ensuring the accuracy, consistency, and integrity of clinical trial data. Professionals in this role check data for errors, discrepancies, and adherence to regulatory standards. They work closely with data management teams, using various validation tools and programming techniques to clean and validate data. This process ensures that clinical trial results are reliable and meet compliance requirements set by agencies like the FDA or EMA.

What does clinical data validation do?

In a Clinical Data Validation role, your daily tasks often include reviewing clinical trial data for accuracy and completeness, identifying and resolving discrepancies, and ensuring compliance with regulatory standards. You may work closely with data managers, biostatisticians, and clinical teams to address data queries and support ongoing data cleaning activities. Additionally, you’ll assist with the development and implementation of data validation plans, perform system checks, and contribute to the preparation of final study databases for analysis. These responsibilities require a high level of precision and a collaborative mindset, as quality data is crucial for the success of clinical research projects.

What are the key skills and qualifications needed to thrive in clinical data validation?

To excel in Clinical Data Validation, a strong background in clinical research, data management, and attention to detail is crucial, often supported by a degree in life sciences or a related field. Familiarity with data validation software, electronic data capture (EDC) systems, and knowledge of regulatory compliance guidelines such as CDISC and GCP are typically required. Excellent analytical thinking, problem-solving skills, and clear communication are vital for collaborating with cross-functional teams. These competencies ensure the accuracy and reliability of clinical trial data, which is essential for regulatory approvals and successful study outcomes.

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Clinical Data Validation jobs near you
Infographic showing various Clinical Data Validation job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, and 3% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $81,651 per year, or $39.3 per hour.

Principal Clinical Data Science Lead

United, PA • Remote

535 ICR Colombia - COL
See more jobs at 535 ICR Colombia - COLexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

Principal Clinical Data Science Lead - United States, Mexico, Colombia (Remote)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We have an incredible opportunity for a Principal Clinical Data Science Lead to join ICON’s Full-Service IOD Clinical Data Science team. The Principal Clinical Data Science Lead (Principal CDSL) leads and serves as the primary contact for end-to-end data review activities performed on clinical trials. They are accountable for achieving clinical data science deliverables on-time, with high-quality, and to agreed financial metrics. The Principal CDSL will serve as the primary point of contact for internal and external team members regarding clinical data review activities and lead these data review activities to ensure delivery of data fit for analysis. They will provide input into clinical system development activities and clinical risk management activities.

Locations: remote or hybrid

  • Mexico
  • Colombia
  • United States

What you will be doing:

  • Develops and oversees timeliness of clinical data science activities during the life cycle of studies as it relates to data review and data delivery milestones
  • Participates in Sponsor and/or third-party audits
  • Forecasts budget, hours, and resourcing for clinical data review activities
  • Performs analytic review as defined in the scope of work and functional plans focusing on errors that matter or have a meaningful impact on the safety of the subject or interpretation of the final analysis
  • Accountable for the development of planning documents related to data review, data analytics, and data deliverables
  • Establishes approach and leads resources to achieve operational and strategic plans
  • Travel (approximately 15%) domestic and/or international

Your profile:

  • 8+ years of clinical data management experience in a clinical research organization or pharmaceutical company
  • 2+ years of experience working in a clinical research organization (CRO)
  • Experience with all steps within the data science lifecycle and most major data science study tasks, with proficiency in at least one Clinical Data Management system required (e.g., Rave, Inform, Oracle Clinical, OCRDC, UX EDC)
  • Strong project management skills with experience leading multiple projects simultaneously
  • Excellent leadership and communication skills
  • Budget and timeline management experience
  • Data Analytic and Data Validation experience
  • Established Mentor and/or SME experience
  • Bachelor’s degree or local equivalent
  • Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write, and speak fluent English and host country language.

* Please submit all applications in English *

#LI-Remote

#LI-TP1


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply