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Scientific Reviewer Jobs in Wisconsin (NOW HIRING)

Bachelor's degree in Chemistry (or related scientific field) with 2+ years' relevant experience (pharmaceutical CMO/CRO). * Knowledge of cGMP and cGLP guidelines for contract manufacturing and ...

SERM Scientific Director Business Introduction At GSK, we have bold ambitions for patients, aiming ... Ensures scientifically sound review and interpretation of data and management of safety issues and ...

WI · On-site

$68 - $115/hr

May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. * Partners with ...

WI · On-site

$68 - $115/hr

May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. * Partners with ...

WI · On-site

$90 - $130/hr

May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. * Partners with ...

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Scientific Reviewer information

What is a scientific reviewer?

A Scientific Reviewer evaluates scientific data, research findings, and technical documents to ensure accuracy, validity, and compliance with regulations or standards. They often work in regulatory agencies, journals, or research organizations, assessing study methodologies, experimental results, and conclusions. Their role is critical in maintaining scientific integrity and ensuring that published or approved research meets established guidelines. Additionally, they may provide recommendations for improvements or further studies based on their evaluations.

What are the typical daily responsibilities of a scientific reviewer?

On a typical day, a Scientific Reviewer evaluates submitted scientific manuscripts, grant proposals, or research protocols for validity, originality, and adherence to ethical standards. They often collaborate with editors, fellow reviewers, and sometimes authors to provide constructive feedback and recommend acceptance, revision, or rejection of submissions. Responsibilities might also include checking data accuracy, reviewing statistical methodologies, and keeping up with current developments in one’s field. This role requires balancing rigorous analysis with clear written communication to support the advancement of quality research.

What are the key skills and qualifications needed to thrive as a scientific reviewer?

To thrive as a Scientific Reviewer, you need a robust background in scientific research, critical analysis, and attention to detail, usually supported by an advanced degree in a scientific discipline. Familiarity with manuscript management systems, statistical analysis software, and databases like PubMed or Web of Science is common. Excellent communication, impartiality, and time management skills help set top Scientific Reviewers apart. These capabilities ensure thorough, objective evaluation of scientific work and timely collaboration within the review process.

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

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

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

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

Infographic showing various Scientific Reviewer job openings in Wisconsin as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 79% Full Time, 16% Part Time, and 3% Contract. Highlights an 74% Physical, 3% Hybrid, and 23% Remote job distribution.

Data Reviewer, Quality Control

Scorpion Therapeutics

Madison, WI • On-site

$95 - $125/hr

Other

Posted 4 days ago


Job description

Responsibilities:
  • Perform independent technical review of internal and external laboratory data
  • Evaluate data for accuracy, completeness, and compliance with GMP and specifications
  • 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/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 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 for trend analysis and system suitability trending
  • Perform additional duties as assigned
Requirements:
  • Bachelor’s degree in chemistry (or any STEM degree) and 5+ years GMP experience, or Master of Science (STEM) with 3+ years in a cGMP laboratory (pharmaceutical CMO/CRO)
  • Experience with analytical data review and documentation practices
  • Working knowledge of analytical methods (HPLC, GC, LC-MS, NMR, FTIR, Appearance, pH, KF, UV spectrometry) and microbiology testing
  • Working knowledge of GMP/GDP and laboratory systems
  • Candidates must have current, valid authorization to work in the country where this role is located.
Preferred:
  • Working knowledge of USP, ISO, FDA, and ICH guidelines
  • Familiarity with LIMS
  • Strong communication skills; solid organization and deadline management
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