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Freelance Qc Data Reviewer Jobs (NOW HIRING)

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 ...

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 ...

Quality Control Data Reviewer ISalary Range: $68,000- 75,000Location: Germantown, MDAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and ...

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 ...

Review quality control testing for compliance with internal SOPs and specifications * Assist in technical data review of the raw data generated for various compendial testing (such as USP/NF, EP, JP ...

The position will also support QA initiatives when necessary and collaborate with laboratory personnel to review data per cGMP compliance and data integrity. The Reviewer should incorporate sound ...

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 ...

Review quality control testing for compliance with internal SOPs and specifications * Assist in technical data review of the raw data generated for various compendial testing (such as USP/NF, EP, JP ...

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 ...

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 ...

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 ...

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 ...

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

As of Sep 11, 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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Infographic showing various Freelance Qc Data Reviewer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% 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.

Quality Control Data Reviewer

Milford, MA • On-site

$90K - $110K/yr

Other

Medical, Retirement

Re-posted 9 days ago


Job description

Advancing medicine to save lives. Together.
Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.
Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients.
Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.
As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.
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 laboratory. Data review may consist of all/some of the following:
• Review and approval of QC test analytics; in process, release, stability, validation
• Track, organize, prepare QC test results for product release
• Review and approval of LIMS test results, labels and stage reports
• Revise SOPs, Forms
• Train employees on cGMP/GDP
Duties and Responsibilities
  • Review and approval of cGMP analytical data comparing results to internal and customer specifications, SOPs, and established standards to ensure accuracy and quality of data
  • Works collaboratively with QC team members and cross functional teams for timely resolution of quality issues to achieve project goals
  • Support Product Release activities ensuring timelines are met
  • Work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors
  • Identify and resolve issues with assistance from Data Review team
  • Review of LIRs
  • Support all data integrity initiatives and strive for right first time
  • Make daily decisions about the quality of data based on biochemical knowledge and compliance background
  • Revise, create SOPS and/or test forms as required
  • Assists with metrics for trending and reporting as required, stability and QC analytical data
  • Task and team-oriented, analytical, organized, detail-oriented, self-motivated and ability to multitask
  • Exceptional communication and interpersonal skills
  • Assists in training of new hires and retraining of QC laboratory staff, as needed
  • Assist/mentor QC new hires on cGMP/GDP
  • Strong knowledge of QC analytical equipment and software required
  • Strong communications skills - written and verbal
  • Able to prioritize workload to meet stringent timelines
  • Provide timely status updates to Management upon request
  • Proficient with MS Outlook, Word, Excel and PowerPoint, and other electronic systems
  • Performs other duties as assigned
Qualifications
  • B.S. in Chemistry, Biology, Chemical Engineering, or related biological sciences
  • 3+ years in a cGMP analytical laboratory environment
  • HPLC, PA800, CS2500, SDS Page
  • LIMS, EMPOWER
  • cGMP experience
Working Conditions
  • Personal protective equipment must be worn in the laboratories according to Rentschler safety requirements
  • Will interact with other departments
  • Pace may be fast and job completion demands may be high
  • Not a hybrid position, work must be performed on site
Physical Requirements
  • May be required to stand for long periods of time while performing review of lab logbooks, equipment, lab documentation
  • Must be able to walk distances between labs, offices, departments
  • Must be able to work safely in a lab environment
  • PPE as required

Base Pay Range
$90,000 - $110,000
Disclosure Statement
Rentschler Biopharma, Inc is committed to fair and equitable compensation practices. The base pay range listed for this position is the anticipated annual base salary range the organization reasonably, and in good faith, expects to pay for this position at this time. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law. The annual base salary is just one component of our Total Rewards package, which also includes our annual discretionary bonus program, medical insurance, our generous 401K program, plus a host of other benefits to aligned to support our employees' personal and professional wellness. The salary pay range is subject to change and may be modified at any time.