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Clinical Data Reviewer Jobs (NOW HIRING)

ICON

Medical Data Reviewer

Medical Data Reviewer 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 ...

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 ...

Faeth Therapeutics

Clinical Data Manager

Austin, TX · 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 ...

Encoded Therapeutics

Clinical Data Manager

$110K - $135K/yr

Review Tables, Figures, and Listings (TFL) specifications and listings to ensure they are fully supported by the clinical data collected. Partner directly with statisticians to investigate document ...

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Clinical Data Reviewer information

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How much do clinical data reviewer jobs pay per hour?

As of Jul 15, 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 biostatistics 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 typically ranges from $50,000 to $80,000 per year, depending on experience, location, and the complexity of the clinical trials. Entry-level reviewers may earn closer to $50,000, while experienced professionals with specialized skills can earn over $80,000. Many roles also offer benefits such as health insurance and opportunities for certification to advance careers.

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 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 does a clinical reviewer do?

A clinical data reviewer evaluates and ensures the accuracy, completeness, and quality of clinical trial data. They review case report forms, monitor data consistency, and may use data management tools to identify discrepancies, supporting regulatory compliance and data integrity in clinical research.

Is CRA an entry level job?

A Clinical Data Reviewer (CDR) role is often considered an entry-level position in clinical research, suitable for candidates with a bachelor's degree in a health or science field. However, some employers prefer candidates with prior experience or familiarity with electronic data capture systems and industry regulations. Advancement typically requires gaining experience and developing skills in data management and regulatory compliance.
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Clinical Data Reviewer jobs near you
Infographic showing various Clinical Data Reviewer job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% 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 Study Data Reviewer

IUVO BIOSCIENCE OPERATIONS, LLC

Rochester, NY

$60K - $74K/yr

Full-time

Posted 13 days ago

Job description

A Trusted CRO Partner for the Future of Eye Care

iuvo Clinical is a full-service ophthalmology-focused contract research organization (CRO) dedicated to improving patient’s quality of life with breakthrough eye care therapies. We combine decades of specialized experience with a high touch, high science approach, partnering with innovators to accelerate ophthalmic breakthroughs from concept to commercialization. Whether advancing a novel retinal therapy or supporting a complex ocular device trial, we provide the expertise, flexibility, and personal dedication to ensure your clinical trial’s success.

We offer a comprehensive benefits package and the opportunity to broaden your experience and grow your career!

We currently have an exciting opportunity for a Data Reviewer.

SUMMARY

The Data Reviewer is responsible for ensuring the accuracy, completeness and consistency of clinical trial data to meet all regulatory standards. The Data Reviewer, in coordination with data management teams, serves to identify and resolve data discrepancies in Electronic Data Capture (EDC) systems throughout the study lifecycle.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Maintain awareness of the pertinent elements of contract and scope of work for assigned project(s) and communicate status updates to the Data Manager (DM) and/or Project Manager (PM) as necessary.
  • Data Review & Quality Control: Review participant-level data, including vision testing results, to ensure adherence to study protocols.
  • Query Management: Identify errors or implausible data and coordinate with study sites or IHCRA/Clinical Research Associates (CRAs) to resolve discrepancies.
  • Review and adhere to the requirements of study-specific DMP for assigned project(s) and update as required.
  • Compliance Monitoring: Ensure all data collection practices align with Good Clinical Practice (GCP), HIPAA regulations, and International Council for Harmonization (ICH) guidelines.
  • In-Stream Trend Analysis: Conduct ongoing analysis and interpretation of data to identify data quality issues, safety signals, or protocol deviations early in the trial
  • Support study-specific database builds, including development of edit checks and perform User Acceptance Testing (UAT).
  • Perform data listing reviews and based on the review, query or apply self-evident corrections or other global rulings permitted in cases where queries are not required, per the Data Management Plan (DMP) for the assigned projects. Resolve answered queries and re-queries where appropriate.
  • Participate in completion of all activities necessary for the finalization and transfer the clinical database and related project documents to the sponsor.
  • Maintain proficiency in DM systems and processes through regular training courses.
  • Understand the coding process.
  • Comprehend the purpose of interim, dry run, data cut.
  • Participate in internal meetings.
  • Attend in-process review meetings.
  • Participate in internal/external audits as required.

QUALIFICATIONS & REQUIREMENTS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required and are not all-inclusive.

EDUCATION and/or EXPERIENCE

  • Bachelor’s degree in a life science or related field preferred or related experience
  • Requires 1–3 years of experience in clinical data review, monitoring, or data management.
  • Knowledge of clinical data, and ICH/Good Clinical Practices.
  • Work experience in clinical research, drug development, data management, or other healthcare environment preferred.
  • Familiarity with medical terminology.
  • Experience in ophthalmology therapeutic area preferred

COMPUTER SKILLS

  • Proficiency in navigating MS Windows, as well as use of MS Word, Excel, and email applications. Excellent speed and accuracy of keyboard skills.
  • Experience with DM practices and relational database management software systems

COMMUNICATION SKILLS

This position requires a person who communicates effectively both verbally and in writing with clinicians, clients, vendors, and internal project team members through demonstration of:   

  • Excellent presentation and interpersonal skills, including clear, succinct, and timely communication to different audiences
  • Sharing ideas in a constructive manner 
  • Listening to and objectively considering ideas and suggestions from others 
  • Keeping others informed of work progress, timetables and issues 
  • Read and comprehend work instructions/SOPs and protocols and write clear, concise communications and documentation 

OTHER SKILLS and ABILITIES

  • Good organizational, planning, and time management skills
  • Ability to multitask under tight deadlines while providing attention to detail.
  • Ability to be flexible and adapt to change.
  • Ability to work independently as well as be part of a multi-disciplinary team.
  • Solid problem-solving skills

PHYSICAL DEMANDS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employee is regularly required to sit or stand at a desk, type, talk, see and hear.

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Office setting / remote home office. iuvo Clinical fosters a video-first environment; employees are expected to have their cameras on for all internal and external meetings, check-ins, and collaborative sessions.

Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

LOCATION Remote

TRAVEL 10%.

DISCLAIMER

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.

iuvo Clinical is an Equal Opportunity Employer