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Clinical Data Reviewer Jobs (NOW HIRING)

Kelly Services

Clinical Data Reviewer

Irving, TX

$50/hr

Clinical Data Reviewer Location: Irving, TX Department: Beauty and Personal Care Work Schedule : M-F; 6:30am-3:30pm AND 9:30am-6:30pm Classification: Full-Time, Contract-to-Hire Benefits: Full ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Support clinical data review requirements from Lead data manager. * Create customise data review listings for study per specifications from lead data manager. * Provide clinical data management ...

Pacer Group

HEDIS Data Reviewer

Philadelphia, PA · On-site

HEDIS Data Reviewer Location: Philadelphia, PA 19113 (Hybrid) Duration: 3 Months Schedule: Standard ... Providing clinical and administrative support to providers as directed. * Maintaining productivity ...

Pacer Group

HEDIS Data Reviewer

Philadelphia, PA · On-site

$40 - $44/hr

HEDIS Data Reviewer Location: Philadelphia, PA 19113, USA Duration: 3 Months Schedule: Standard ... Providing clinical and administrative support to providers as directed. * Maintaining productivity ...

Belcan

Clinical Data Manager

Durham, NC

$55 - $65/hr

Clinical Data Manager Location: Durham, NC Duration: 09 Months contract (Potential temp to Perm ... Performs User Access Management in Veeva vault EDC, create specifications for data review listings ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · Remote

$125K - $175K/yr

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M ... Review and contribute to key study documents, including: * Data Management Plans (DMPs) * Case ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · On-site

$125K - $175K/yr

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M ... Review and contribute to key study documents, including: * Data Management Plans (DMPs) * Case ...

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Clinical Data Reviewer information

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How much do clinical data reviewer jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for clinical data reviewer in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $36.30 per hour, depending on experience, location, and employer.

How to become a clinical data reviewer?

To become a clinical data reviewer, candidates typically need a bachelor's degree in health sciences, life sciences, or a related field. Relevant experience in clinical research, data management, or clinical trial processes is often required, along with proficiency in data analysis tools like SAS or SQL. Certifications such as the Society for Clinical Data Management (SCDM) Certified Data Manager can enhance job prospects.

How much does a clinical data reviewer make?

The average salary for a clinical data reviewer ranges from $50,000 to $80,000 per year, depending on experience, location, and the complexity of the data reviewed. Entry-level positions typically start around $45,000, while experienced reviewers with specialized skills can earn over $90,000 annually. Many roles require familiarity with electronic data capture systems and relevant certifications such as CDISC or CDM.

What are some common day-to-day responsibilities of a Clinical Data Reviewer?

As a Clinical Data Reviewer, your daily tasks often include evaluating and verifying clinical trial data for completeness, consistency, and accuracy according to study protocols and regulatory requirements. You'll collaborate closely with data managers, clinical research associates, and biostatisticians to resolve discrepancies and ensure data quality. Reviewing case report forms (CRFs), providing feedback on data queries, and documenting findings are typical activities. This role requires ongoing communication and teamwork to maintain timelines and support the integrity of the clinical trial process.

What is a Clinical Data Reviewer job?

A Clinical Data Reviewer is responsible for ensuring the accuracy, consistency, and integrity of clinical trial data. They review patient data in clinical databases, identify discrepancies, and collaborate with data management and clinical teams to resolve issues. Their role is critical in ensuring that trial data meets regulatory standards and supports reliable study outcomes. Clinical Data Reviewers typically have backgrounds in life sciences, clinical research, or data management.

What jobs pay 2000 a day?

Clinical Data Reviewers typically do not earn $2000 a day; such high daily rates are usually associated with highly specialized or consulting roles in fields like executive consulting, legal, or financial services. Some freelance or contract professionals with extensive experience and niche expertise may command high daily rates, but these are uncommon in standard clinical data review positions. Most clinical data reviewer roles offer salaries or hourly wages significantly below this level.

What are the key skills and qualifications needed to thrive in the Clinical Data Reviewer position, and why are they important?

To thrive as a Clinical Data Reviewer, you typically need a background in life sciences, experience with clinical research processes, and a keen eye for detail when reviewing clinical trial data. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and compliance frameworks like Good Clinical Practice (GCP) or CDISC standards is highly valued. Strong analytical thinking, effective communication, and the ability to collaborate across multidisciplinary teams are standout soft skills in this role. These competencies are crucial for ensuring the accuracy, reliability, and regulatory compliance of clinical data, ultimately supporting successful research outcomes.

What is the role of a clinical data reviewer?

A clinical data reviewer is responsible for examining and validating data collected during clinical trials to ensure accuracy, completeness, and compliance with regulatory standards. They analyze datasets, identify discrepancies, and collaborate with study teams to maintain data integrity, often using electronic data capture systems and adhering to Good Clinical Practice (GCP) guidelines.
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What cities are hiring for Clinical Data Reviewer jobs? Cities with the most Clinical Data Reviewer job openings:
What are the most commonly searched types of Clinical Data Reviewer jobs? The most popular types of Clinical Data Reviewer jobs are:
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What job categories do people searching Clinical Data Reviewer jobs look for? The top searched job categories for Clinical Data Reviewer jobs are:
Clinical Data Reviewer jobs near you
Infographic showing various Clinical Data Reviewer job openings in the United States as of June 2026, with employment types broken down into 3% Locum Tenens, 4% As Needed, 1% Full Time, 75% Part Time, 3% Temporary, and 14% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.
Clinical Data Reviewer

Clinical Data Reviewer

Kelly Services

Irving, TX

$50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago

Job description

Clinical Data Reviewer
Location: Irving, TX
Department: Beauty and Personal Care
Work Schedule: M-F; 6:30am-3:30pm AND 9:30am-6:30pm
Classification: Full-Time, Contract-to-Hire
Benefits: Full benefits package
Salary: $50-60K; DOE
Reports To: Quality Assurance Manager
Position Summary
We are seeking a detail-oriented Clinical Data Reviewer to join our Beauty and Personal Care clinical trials team in Irving, TX. In this role, you will be responsible for reviewing and ensuring the integrity, safety, and regulatory compliance of all clinical trial data, processes, and laboratory environments. This position strictly adheres to current Good Clinical Practices (GCP) and internal Standard Operating Procedures (SOPs).
Key Responsibilities
Daily Lab & Environment Monitoring
  • Verify and audit patch booths before testing begins to ensure correct patch types, testing conditions, and test article applications.
  • Monitor, verify, and log temperatures and humidity levels for the retain closet, test article closet, drug closet, server room, archive room, incubators, refrigerators, and freezers.
  • Ensure all balances are completely level and verify calibration logs.
  • Maintain, organize, and file all environmental and operational logs in their respective binders.
  • Secure and maintain keys to all restricted facility areas.
Study Compliance & Data Auditing
  • Conduct in-study audits and review Informed Consent Forms (ICFs) and Medical History Forms for completeness.
  • Review Study Administrative Notebooks and regulatory binders prior to the start of any clinical trial.
  • Audit data sheets, data tables, and statistical analysis results to ensure absolute accuracy.
  • Review serious and non-serious Adverse Events (AEs) to safeguard participant safety and data accuracy.
  • Witness jar fills prior to study initiation when applicable.
Inventory & Equipment Management
  • Inventory incoming test articles, maintain accurate accountability logs throughout the study lifecycle, and log retain samples.
  • Ensure facility equipment (timers, pipettes, thermometers) and standard weights are checked for monthly calibration and expiration.
  • Coordinate the semi-annual certification checks for facility Fume Hoods.
Documentation & Support
  • Maintain standard operating procedures (SOPs), standard training procedures (STPs), employee training records, CV binders for physicians, and employee acknowledgment logs.
  • Assist the QA Manager or QA Coordinator II in authoring new SOPs and updating existing ones.
  • Attend protocol and study status meetings to provide timely quality updates.
Health, Safety, & Environment (HSE)
  • Actively participate in the site safety program to maintain a zero-injury work environment.
  • Utilize necessary HSE precautions and Personal Protective Equipment (PPE) when working with chemicals, cosmetic test articles, and unknown hazards.
  • Monitor, enforce, and report unsafe conditions or personal injuries in compliance with company policies and government regulations.
Qualifications & Requirements
Education & Experience
  • Bachelor’s Degree (BA/BS) from a four-year college or technical school; OR 6 months to 1 year of related experience and/or training; OR an equivalent combination of education and experience.
Certifications & Licenses (Preferred)
  • Current certification in Human Protections
  • Current certification in Good Clinical Practices (GCP)
  • Current certification in Bloodborne Pathogens
Core Competencies & Skills
  • Technical & Computer Skills: Proficiency with Microsoft Office (Word, Excel, Outlook) and Database software (FileMaker Pro).
  • Attention to Detail: Proven thoroughness in monitoring quality standards and reviewing complex data tables.
  • Organization & Planning: Excellent prioritization skills with the flexibility to manage changing clinical priorities.
  • Communication: Strong verbal and written communication skills; ability to collaborate ethically and professionally across teams.
For immediate consideration, please forward your updated resume.
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