ZipRecruiter

Log In

1

Clinical Data Reviewer Jobs (NOW HIRING)

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It ... Gather cross-functional input to drive creation of custom data review plans. Evaluate options and ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It ... Gather cross-functional input to drive creation of custom data review plans. Evaluate options and ...

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

Ensure the delivery of high-quality, complete, and reliable clinical data through effective data review, issue management, and quality oversight. * Drive timely database lock and submission-ready ...

Jj

Analyst II, Clinical Data Manager

Raritan, NJ · On-site

Review clinical data management documents (including submission package) for appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Ensure compliance with ...

Collabera

Clinical Data Manager

Irvine, CA

Ensure study data quality by CRF data review, preparation for entry, query processing, discrepancy ... Clinical Database Systems Knowledge - EDC and Paper Intermediate to Advanced level proficiency with ...

next page

Showing results 1-20

All JobsClinical Data Reviewer Jobs

Clinical Data Reviewer information

See salary details

$12

$26

$43

How much do clinical data reviewer jobs pay per hour?

As of Jul 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 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.
More about Clinical Data Reviewer jobs
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:
What states have the most Clinical Data Reviewer jobs? States with the most job openings for Clinical Data Reviewer jobs include:
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 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.
Data Reviewer, Quality Control

Data Reviewer, Quality Control

Arrowhead Pharmaceuticals

Verona, WI • On-site

$80K - $90K/yr

Full-time

Posted 13 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
The Data Reviewer independently performs technical review of laboratory data and documentation to ensure compliance with analytical methods, specifications, GMP/GDP requirements, and data integrity standards. This role exercises independent judgment in evaluating data quality, identifying discrepancies, and resolving routine to moderately complex compliance issues. The Data Reviewer supports inspection readiness activities, contributes to continuous improvement initiatives, and serves as a technical resource to junior team members.
Responsibilities
  • Perform independent technical review of internal data and external laboratory data
  • Evaluate data for accuracy, completeness, and compliance with GMP and specifications
  • Independently evaluate, investigate, and document discrepancies, atypical results, and documentation inconsistencies to determine impact and ensure appropriate resolution
  • Review routine release and stability data, method validation data and report, IPC data, cleaning samples, and logbooks for traceability and compliance
  • Communicate and collaborate with laboratory staff and CDMOs to resolve data quality issues
  • Support audit readiness activities and participate in inspections
  • Maintain knowledge of laboratory systems and software for effective review
  • Recommend and support implementation of improvements to data review processes, documentation practices, and workflow efficiency
  • Provide guidance and onboarding support to junior reviewers on review practices, documentation standards, and GMP expectations
  • Embrace digital tools and opportunities for trend analysis, system suitability trending.
  • Perform additional duties as assigned in support of operations

Requirements
  • Bachelor's degree in chemistry or (any STEM degree) and 5+ years GMP experience, or a Master of Science (STEM degree) with minimum 3 years of experience in a cGMP laboratory (pharmaceutical CMO/CRO).
  • Experience with analytical data review and documentation practices
  • Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR, Appearance, pH, KF, UV spectrometry and microbiology testing.
  • Working knowledge of GMP/GDP and laboratory systems

Preferred
  • Working knowledge of USP, ISO, FDA and ICH guidelines
  • Familiarity with laboratory information systems, LIMS.
  • Strong verbal and written communication skills and ability to work with diverse professionals in a matrix environment.
  • Solid organizational skills with ability to adapt to changing priorities and deadlines.

Wisconsin pay range
$80,000-$90,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
California Applicant Privacy Policy

Apply