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Clinical Data Reviewer Jobs in Wisconsin (NOW HIRING)

Deloitte

Clinical Data AMS Sr. Consultant

Milwaukee, WI · On-site

Provide operational and functional support for eClinical Elluminate, including data review workflows, listings/reports configuration, and integration touchpoints with upstream/downstream clinical ...

New

Wisconsin

Clinical Research Data Specialist

Madison, WI · On-site

$62K/yr

Data Engineer I Job Summary: The Department of Orthopedics and Rehabilitation is seeking a Clinical ... Application reviewers will rely on these written materials to determine which applicants move ...

Elephas

Senior Data Scientist

Madison, WI · On-site

The Senior Data Scientist will support clinical correlation data modeling, which includes working ... Provide technical leadership through code review, methodological guidance, and best-practice ...

Elephas

Senior Data Scientist

Madison, WI

The Senior Data Scientist will support clinical correlation data modeling, which includes working ... Provide technical leadership through code review, methodological guidance, and best-practice ...

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Clinical Data Reviewer information

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How much do clinical data reviewer jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for clinical data reviewer in Wisconsin is $26.49, according to ZipRecruiter salary data. Most workers in this role earn between $14.57 and $36.63 per hour, depending on experience, location, and employer.

What is a clinical data reviewer?

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 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 are the key skills and qualifications needed to thrive as a clinical data reviewer?

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 are the most commonly searched types of Clinical Data Reviewer jobs in Wisconsin?

The most popular types of Clinical Data Reviewer jobs in Wisconsin are:

What are popular job titles related to Clinical Data Reviewer jobs in Wisconsin?

For Clinical Data Reviewer jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Clinical Data Reviewer jobs in Wisconsin look for?

The top searched job categories for Clinical Data Reviewer jobs in Wisconsin are:

Clinical Data Reviewer jobs near you
Infographic showing various Clinical Data Reviewer job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $55,094 per year, or $26.5 per hour.

Data Reviewer, Quality Control

Arrowhead Pharmaceuticals

Madison, WI • On-site

$80K - $90K/yr

Full-time

Re-posted 24 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.

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