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Pharmaceutical Data Review Jobs (NOW HIRING)

Eurofins

Group Leader- Data Review

Columbia, MO · On-site

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and ... Data Review & Compliance * Review GMP data for accuracy, completeness, and compliance with ...

Eurofins

Scientist: Data Review

Lancaster, PA · On-site

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and ... Reviewing laboratory documentation for accuracy, consistency, and clarity. * Gain a technical ...

RXinsider LTD.

Review analytical data, chromatographic reports, calculations, and laboratory worksheets for ... Minimum 2 years' experience in a regulated pharmaceutical analytical laboratory, or equivalent ...

RXinsider LTD.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and ... Reviewing laboratory documentation for accuracy, consistency, and clarity. * Gain a technical ...

ARL Bio Pharma

$23 - $28/hr

Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug ... The Data Review Chemist II will independently apply technical aptitude and experience to ...

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Pharmaceutical Data Review information

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How much do pharmaceutical data review jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for pharmaceutical data review 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.

What is the difference between Pharmaceutical Data Review vs Pharmaceutical Data Analyst?

AspectPharmaceutical Data ReviewPharmaceutical Data Analyst
Required CredentialsBachelor's degree in life sciences or related field; knowledge of regulatory standardsBachelor's or master's in data science, statistics, or related field; analytical skills
Work EnvironmentRegulatory agencies, pharmaceutical companies, clinical trial settingsData-focused roles within pharmaceutical or biotech companies, research labs
Employer & Industry UsageUsed to ensure compliance, review clinical data, and prepare regulatory submissionsUsed to analyze data trends, generate reports, and support decision-making

Pharmaceutical Data Review primarily involves evaluating clinical and regulatory data for compliance and accuracy, often within regulatory or clinical settings. In contrast, Pharmaceutical Data Analysts focus on analyzing large datasets to identify trends and support business decisions. Both roles require strong analytical skills but differ in their core responsibilities and work environments.

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Pharmaceutical Data Review jobs near you
Infographic showing various Pharmaceutical Data Review job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 83% Full Time, 12% Part Time, and 3% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

Scientist, Data Review

Columbia, MO • On-site

Eurofins Scientific
Scientific Research and Development Services • 10K+ employees
Learn more about Eurofins Scientificexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired 2 days ago. Applications are no longer accepted.

Key responsibilities

  • Review scientific reports to ensure regulatory requirements are met, data is accurate, and reports are of high quality.

  • Assist with internal audits.

  • Work closely with lab operations staff and have the authority for final report sign-off.

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 181 frontline employees who took The Breakroom Quiz

Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

*THIS IS NOT A DATA SCIENCE POSITION*

Eurofins BPT-Columbia is looking for a Associate Scientist, Data Review to join our Quality Assurance team located in Columbia, Missouri.  The Quality Assurance Associate position is an entry-level position involved in day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). 

  • Review scientific reports under cGMP guidelines to ensure regulatory requirements have been met, the data is whole and accurate, and the report is of high quality.
  • Assisting with internal audits
  • Work closely with lab operations staff on a day-to-day basis and have the authority and responsibility for final report sign-off.
  • Other duties as assigned.
Qualifications

The ideal candidate would possess:

  • Experience in a laboratory setting or GMP pharmaceutical setting.
  • Good organizational skills; ability to follow direction and good communication skills are required.
  • Strong computer, scientific, and organizational skills.
  • Excellent communication (oral and written) and attention to detail.
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

Minimum Qualifications

  • Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas.
Additional Information

Position is full-time position, Monday - Friday 8:00am - 4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

To learn more about Eurofins, please explore our website www.eurofinsus.com.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

Pay

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Hours and flexibility

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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