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Freelance Qc Data Reviewer Jobs (NOW HIRING)

Eurofins

QC Data Reviewer - LNP and Lipids

Boston, MA · On-site

This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations.

ARL Bio Pharma

QC Data Review Chemist

Oklahoma City, OK

$23 - $28/hr

With moderate guidance, the Data Review Chemist II is responsible for utilizing the Quality Management System (QMS) standard operating procedures (SOP) and work instructions (WI) to perform quality ...

Clearspeed

Quality Control Data Analyst

$96K - $134K/yr

Review, evaluate, and accurately label audio recordings and other data files using designated software tools and quality control procedures. * Inspect, classify, and analyze data according to ...

Actalent

Data Reviewer

Verona, WI · On-site

$35 - $43/hr

You will collaborate with QC chemists to address any data or reporting issues and escalate ... Review method validation data for accuracy, integrity, and regulatory compliance. * Work with ...

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Freelance Qc Data Reviewer information

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How much do freelance qc data reviewer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for freelance qc 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.

What is a freelance QC data reviewer?

Freelance QC (Quality Control) Data Reviewers are independent professionals who review and verify data for accuracy, completeness, and compliance with regulations or project specifications. They typically work on a contract basis for organizations in industries such as pharmaceuticals, clinical research, or manufacturing. Their main responsibilities include checking data sets, identifying errors or inconsistencies, and ensuring that quality standards are met before data is finalized or submitted. Freelance QC Data Reviewers must have strong attention to detail and a solid understanding of relevant industry guidelines.

What are the key skills and qualifications needed to thrive as a freelance QC data reviewer?

A Freelance QC Data Reviewer needs a strong background in data analysis, quality control principles, and expertise in industry-specific guidelines, often supported by a relevant degree or experience in clinical research or pharmaceuticals. Familiarity with electronic data capture (EDC) systems, statistical software, and compliance tools such as Good Clinical Practice (GCP) or FDA regulations is typically required. Attention to detail, critical thinking, and effective communication skills help reviewers identify discrepancies and collaborate with project stakeholders. These abilities are crucial to ensuring data integrity, regulatory compliance, and the overall quality of project deliverables.

What are some common challenges faced by freelance QC data reviewers when working with multiple clients?

Freelance QC Data Reviewers often juggle projects from different clients, each with their own protocols and data standards. One common challenge is quickly adapting to varying quality control guidelines, documentation formats, and review tools. Managing deadlines across several projects can also be complex, requiring strong organizational and communication skills. Building clear expectations with clients and maintaining meticulous records helps ensure accuracy and client satisfaction in a fast-paced, remote work environment.

What is the difference between Freelance Qc Data Reviewer vs Clinical Data Coordinator?

AspectFreelance Qc Data ReviewerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in data reviewRequires a degree in health sciences, nursing, or related field, often with additional certifications
Work EnvironmentRemote, project-based, often freelance or contract rolesUsually in clinical settings or research organizations, sometimes remote
Industry UsageCommon in pharmaceutical, biotech, and CROs for data quality assuranceUsed in clinical research sites, hospitals, and research organizations for data management

The Freelance Qc Data Reviewer primarily focuses on reviewing and ensuring the accuracy of clinical trial data, often working remotely on a contract basis. In contrast, the Clinical Data Coordinator manages data collection, entry, and organization within clinical trials, often working on-site or in a clinical setting. Both roles require knowledge of clinical data processes but differ in scope, responsibilities, and work environment.

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Freelance Qc Data Reviewer jobs near you
Infographic showing various Freelance Qc Data Reviewer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

QC Data Reviewer - LNP and Lipids

Eurofins

Boston, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago

Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

68th of 120 rated laboratories

Job description

Company Description
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!
Job Description
This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations. The role requires attention to detail, familiarity with GMP practices, and the ability to ensure data integrity and regulatory compliance.
  • Review analytical data packages from stability studies, method development, and investigations for LNP and lipid-based products.
  • Evaluate OOS/OOT investigation reports for completeness, scientific soundness, and appropriate corrective actions.
  • Verify calculations, data transcriptions, and chromatographic data for accuracy and compliance.
  • Ensure documentation adheres to GMP and applicable regulatory guidelines.
  • Maintain review timelines and tracking logs to support release and regulatory submission deadlines.
  • Partner with analytical and quality teams to resolve data discrepancies and review findings.

Qualifications
Minimum Required Qualifications:
  • B.S. in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field with 3-4 years of analytical laboratory experience in a GMP-regulated pharmaceutical or biopharmaceutical environment.
  • Proficiency in GMP regulations and Good Documentation Practices.
  • Understanding of how chromatography is operated and how to interpret the data
  • Strong organizational skills, attention to detail, and accuracy in documenting results.
  • Strong time management and multitasking abilities.
  • Ability to work independently and collaborate in a cross-functional environment.
  • Effective communication and documentation skills.

Preferred Qualifications:
  • Experience with chromatograms and the ability to interpret chromatographic data such as HPLC, UPLC, and LC-MS (experience with chromatography data review is a plus).
  • Familiarity with LNP and lipid technologies and investigations.
  • Experience with method development.
  • Experience with software systems such as SLIM, Veeva, JMP, and LIMS.
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information
Additional Details:
The position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Annual rate is between $36.00-$40.00, depending on education and experience

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

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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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