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Freelance Qc Data Reviewer Jobs (NOW HIRING)

Pharmaron

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Data Reviewer I Salary Range: $68,000- 75,000 Location : Germantown, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...

Rentschler

Quality Control Data Reviewer

Milford, MA · Hybrid

$90K - $110K/yr

  • Medical

  • Retirement

As part of the Milford site's Quality Control team, the Data Reviewer is responsible for the cGMP analytical data review and documentation generated during laboratory analysis in the quality control ...

TOLMAR

QC Data Reviewer III

Fort Collins, CO · On-site

Authorize all sample data in the notebook as well as the associated data repositories (Endeavor and LIMS). * Perform review of chemist reports generated in the laboratory. * Assist the QC trainers by ...

Pharmaron

Quality Control Data Reviewer I

Germantown, MD

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Data Reviewer I Salary Range : $68,000- 75,000 Location : Germantown, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...

Avid Bioservices

Data Reviewer, Quality Control

Tustin, CA

$32.30 - $40.38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Data Reviewer, Quality Control 's main responsibility will be to review Quality Control analytical data. In this role you will: * Conduct a comprehensive and critical evaluation on QC data in ...

CEDENT

Data Reviewer, Quality Control

Verona, WI

The Data Reviewer is responsible for ensuring the completion, quality, and compliance of laboratory data and reports produced within the Quality Control (QC) team. This includes the technical review ...

Avid Bioservices

Data Reviewer, Quality Control

Tustin, CA · On-site

$32.30 - $40.38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Data Reviewer, Quality Control 's main responsibility will be to review Quality Control analytical data. In this role you will: * Conduct a comprehensive and critical evaluation on QC data in ...

AMRI

Data Reviewer III

Rensselaer, NY · On-site

  • Retirement

Quality Control Data Reviewer III - Onsite position in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing ...

Curia, Inc.

Data Reviewer III

Rensselaer, NY · On-site

  • Retirement

Quality Control Data Reviewer III - Onsite position in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing ...

Curia, Inc.

Data Reviewer III

Rensselaer, NY · On-site

  • Retirement

Quality Control Data Reviewer III - Onsite position in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing ...

ARL Bio Pharma

$23 - $28/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

ARL Bio Pharma

QC Data Review Chemist

Oklahoma City, OK

$23 - $28/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Thorne

Quality Control Data Associate

Summerville, SC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assemble, review, and maintain Quality Control laboratory data to support accurate product disposition and timely material release. * Generate Certificates of Analysis (COAs) and other quality ...

Thorne

Quality Control Data Associate

Summerville, SC

$20/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assemble, review, and maintain Quality Control laboratory data to support accurate product disposition and timely material release. * Generate Certificates of Analysis (COAs) and other quality ...

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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 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.

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 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 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.
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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.

Quality Control Data Reviewer I

Pharmaron

Germantown, MD • On-site

$68K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

Position: Quality Control Data Reviewer I
Salary Range: $68,000- 75,000
Location: Germantown, MD
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
What You'll Do
  • Perform comprehensive quality review of bioanalytical assay data for accuracy, completeness, data integrity, and compliance with GLP/GCP requirements, study protocols, SOPs, and client expectations.
  • Review datasets generated from method development, method validation, and sample analysis studies.
  • Review study reports, protocols, protocol amendments, and supporting documentation for accuracy and compliance.
  • Review sample management documentation and verify samples are appropriately documented and stored in LIMS.
  • Review laboratory equipment calibration records, logbooks, and other quality documentation.
  • Ensure laboratory records and documentation accurately reflect actual laboratory activities and events.
  • Work closely with analysts and scientific staff to investigate and resolve data discrepancies, sample management questions, and documentation issues.
  • Maintain accurate QC review records in accordance with SOPs and quality best practices.
  • Initiate and coordinate quality events in TrackWise with Lead Scientists.
  • Communicate with management and internal departments regarding data review findings and study status.
  • Support the development and revision of SOPs, work instructions, methods, study plans, and training materials.
  • Assist with training and mentoring team members as appropriate to experience level and qualification.
  • Track QC metrics, identify recurring errors or trends, and contribute to continuous improvement initiatives that enhance quality and efficiency.
  • Support internal and external audits and maintain awareness of applicable regulatory requirements and industry best practices.
  • Complete required training within established timelines and maintain compliance with laboratory safety policies.

What We're Looking For
  • Bachelor's degree in a relevant scientific field.
  • QC Data Reviewer I: Some laboratory or quality experience.
  • QC Data Reviewer II: 2+ years of relevant quality experience.
  • QC Data Reviewer III: 5+ years of relevant quality experience.
  • Experience working in a Quality Control or Quality Assurance capacity within a bioanalytical laboratory preferred.
  • Experience working in a regulated laboratory environment.
  • Knowledge of GLP, GCP, 21 CFR Part 11, 21 CFR Part 58, and ICH guidelines.
  • Strong attention to detail, organizational skills, critical thinking, and problem-solving abilities.
  • Strong written and verbal communication skills.
  • Strong computer skills, particularly Microsoft Word and Excel, including intermediate to advanced knowledge of Excel formulas and functions.
  • Experience with LIMS, laboratory/instrument software, and quality management systems preferred.
  • Experience with TrackWise or similar quality systems preferred.
  • Experience with project management tools such as Smartsheet preferred.
  • Ability to work independently while collaborating effectively with scientists, analysts, and cross-functional teams.
  • For senior-level roles, demonstrated ability to handle complex data-review issues, mentor team members, support process improvements, and represent the QC function during audits.

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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