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Bioanalytical Data Reviewer Jobs (NOW HIRING)

Pharmaron

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

What You'll DoPerform comprehensive quality review of bioanalytical assay data for accuracy, completeness, data integrity, and compliance with GLP/GCP requirements, study protocols, SOPs, and client ...

Labcorp

Bioanalytical Lead Scientist I

Madison, WI · On-site

Review, analyze, and communicate bioanalytical data and PK results to cross-functional teams and management. * Mentor junior scientists and contribute to the development of bioanalytical capabilities ...

Frontage Laboratories

QC Manager

Exton, PA · On-site

The QC Manager leads a team of QC reviewers responsible for data verification, review of assay outputs, documentation accuracy, and compliance across all GLP bioanalytical studies. Key ...

TCWGlobal

Bioanalytical Scientist

San Diego, CA · On-site +1

$54.48/hr

Bioanalytical Scientist Pay Rate: Up to $54.48/hour Duration: 12-Month Assignment Hours: Full-Time ... Prepare, review, and maintain protocols, records, data summaries, reports, and related ...

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How much do bioanalytical data reviewer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for bioanalytical 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 does a bioanalytical data reviewer do?

A Bioanalytical Data Reviewer is responsible for reviewing and verifying the accuracy, integrity, and compliance of analytical data generated in bioanalytical laboratories. They ensure that all data complies with regulatory requirements and standard operating procedures, often working with data from drug development or clinical trials. This role involves identifying discrepancies, ensuring proper documentation, and supporting audits or inspections by regulatory authorities. The reviewer plays a critical part in maintaining data quality and supporting the reliability of scientific results.

What are some common challenges faced by bioanalytical data reviewers and how can they be managed?

Bioanalytical Data Reviewers often encounter challenges such as managing large volumes of complex data, ensuring data integrity, and meeting tight project deadlines. Attention to detail is crucial, as even minor errors can impact study results and regulatory compliance. Collaborating closely with laboratory analysts and project managers helps address discrepancies efficiently, while proper use of data management systems streamlines the review process. Staying organized and proactive in communication are key strategies for managing these challenges effectively.

What are the key skills and qualifications needed to thrive as a bioanalytical data reviewer, and why are they important?

To thrive as a Bioanalytical Data Reviewer, you need a strong background in analytical chemistry, data analysis, and regulatory standards, typically supported by a degree in life sciences or chemistry. Familiarity with laboratory information management systems (LIMS), chromatographic data systems (such as Empower or Analyst), and compliance with GLP/GCP guidelines is essential. Attention to detail, critical thinking, and effective communication are key soft skills for ensuring data accuracy and collaborating with laboratory teams. These skills are vital for maintaining data integrity, meeting regulatory requirements, and supporting high-quality scientific outcomes.

What is the difference between Bioanalytical Data Reviewer vs Bioanalytical Laboratory Technician?

AspectBioanalytical Data ReviewerBioanalytical Laboratory Technician
CredentialsBachelor's degree in life sciences, experience in data reviewAssociate's or Bachelor's degree, laboratory experience
Work EnvironmentReviewing data, ensuring compliance, documentationPerforming laboratory tests, preparing samples
Industry UsageRegulatory submissions, data integritySample processing, assay execution

The Bioanalytical Data Reviewer primarily focuses on reviewing and validating data generated in the lab, ensuring accuracy and compliance with regulations. In contrast, the Bioanalytical Laboratory Technician is involved in performing laboratory tests and preparing samples. Both roles require scientific knowledge, but the Data Reviewer emphasizes data integrity and documentation, while the Technician handles hands-on testing tasks.

What are popular job titles related to Bioanalytical Data Reviewer jobs?

For Bioanalytical Data Reviewer jobs, the most frequently searched job titles are:

Infographic showing various Bioanalytical Data Reviewer job openings in the United States as of September 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

Associate Director, Bioanalytical Sciences

South San Francisco, CA

Alector
Biotechnology Research and Development • 201 - 500 employees
Learn more about Alectorexternal

$200K - $232K/yr

Full-time

Posted 6 days ago

Job description

Our mission is to develop therapies that empower the immune system to combat neurodegeneration and our team is focused on developing treatments for some of the most challenging diseases facing our society. By harnessing advancements in genetics, immunology and neuroscience, we are pioneering the development of potential therapies to counteract the devastating progression of neurodegeneration. We are supported in this mission by experienced and accomplished scientists and clinicians, a novel portfolio of programs, leading healthcare investors, and pharma company partners, who share in our commitment to bettering the lives of patients and realizing a world where we make brain disorders history.

This role is based at Alector’s headquarters in South San Francisco, CA. Regular onsite presence is essential given the combination of hands-on laboratory work, scientific leadership, and close collaboration with multidisciplinary teams
 

As an Associate Director, Bioanalytical Sciences you will provide strategic and hands-on scientific leadership for bioanalytical activities across Alector’s nonclinical and clinical programs. This role combines portfolio-level bioanalytical strategy with direct laboratory engagement and independent assay development. 

Leverage your deep expertise in ligand-binding assays for pharmacokinetics, and immunogenicity assessments across a range of biological matrices, comfortably move between the hands-on laboratory work and scientific and people leadership. This role encompasses bioanalytical strategy, independent assay development, optimization, and troubleshooting at the bench, CRO oversight, data interpretation and operational decision-making for the group rather than simply coordinating or delegating activities. 

Key Goals & Accountabilities

  • Define and drive bioanalytical strategy across programs! Develop fit-for-purpose Pharmacokinetic, Pharmacodynamic, immunogenicity, and biomarker strategies that address key scientific questions, anticipate assay needs, identify risks early, and support timely nonclinical and clinical program decisions. 

  • Lead assay development and stay hands-on in the laboratory! Independently design, develop, optimize, troubleshoot, and qualify ligand-binding assays using both ELISA and MSD platforms, with proven experience developing assays for antibodies, including PK, ADA, and neutralizing antibody assays. 

  • Translate bioanalytical data into clear scientific decisions! Interpret complex results across programs, communicate findings and risks to multidisciplinary teams, and author or critically review high-quality bioanalytical plans, technical reports, study reports, and related scientific documentation. 

  • Partner across functions and proactively align expectations! Work with Research, Toxicology, and Clinical Development to align Bioanalytical Sciences priorities, timelines, and capacity with program needs, protecting the team from conflicting demands while continuously improving processes, SOPs, and documentation standards. 

  • Lead and develop the team! Build a culture of scientific rigor, accountability, and respect where team members feel comfortable raising questions and challenging assumptions; mentor scientists at all experience levels in a way that removes barriers rather than adding to their workload. 

  • Build strong external bioanalytical partnerships! Apply a strong understanding of GLP and bioanalytical guidelines when participating in the evaluation and selection of CROs for nonclinical and clinical assay validation and sample analysis; develop robust human bioanalytical assays for transfer to CROs and provide scientific oversight of method transfer, validation, sample analysis, troubleshooting, deviations, data quality, timelines, and final study reports. Hold vendors accountable for quality and timelines while maintaining productive professional partnerships. 

  • Strengthen our bioanalytical capabilities! Develop scientists, establish high standards for experimental rigor and data integrity, and integrate innovative technologies, including laboratory automation, AI, and large language models, to accelerate programs, improve quality, and use resources more effectively! 

Required Qualifications

  • PhD in Biology, Pharmacology, Immunology, Biochemistry, or a related scientific discipline with 8–10 years of biotechnology, CRO or pharmaceutical industry experience following completion of the PhD; alternatively, MS/MSc with 12–15  years of relevant industry experience following graduate training. 

  • Extensive hands-on expertise in both ELISA and MSD assay development, including proven independent experience developing, optimizing, troubleshooting, qualifying, and validating ligand-binding assays for measurement of antibodies and/or bispecific antibodies in biological matrices, together with deep expertise in anti-drug antibody (ADA) and neutralizing antibody (NAb) assay development for biologic therapeutics. 

  • Demonstrated experience developing human bioanalytical assays for transfer to CROs, overseeing external assay validation and sample analysis, interpreting complex bioanalytical data, and authoring high-quality technical and bioanalytical study reports. 

  • Strong working knowledge of current FDA and EMA regulatory guidance and industry expectations for bioanalytical method development, validation, immunogenicity assessment, and regulated bioanalysis, with demonstrated ability to translate these expectations into appropriate assay strategies and execution. 

  • Demonstrated ability to establish bioanalytical strategy across multiple programs while remaining hands-on in the laboratory; experience leading and developing scientists; ability to succeed in a fast-paced, multidisciplinary environment with shifting timelines and priorities. 

  • Self-motivated, deadline oriented, and comfortable making sound decisions with incomplete information, learning new skills, troubleshooting independently, and adjusting approach as priorities and data evolve. 

  • Hands-on experience using Benchling as an electronic laboratory notebook and maintaining complete, timely, and rigorous electronic laboratory records; and active use of large language models (LLMs) with a strong interest in evolving AI technologies. 

Preferred Qualifications

  • Experience developing bioanalytical assays, including hybrid ELISA approaches, for siRNA, oligonucleotide therapeutics, or antibody-conjugated siRNA/oligonucleotide modalities. 

  • Experience developing and implementing biomarker assays to support nonclinical or clinical programs. 

  • Experience with Watson LIMS or a comparable bioanalytical laboratory information management system. 

  • Experience with automated liquid- or sample-handling platforms such as Hamilton or Tecan. 

  • Experience introducing new bioanalytical technologies, automation, or data-analysis approaches into laboratory workflows. 

At Alector, our vision is bold, people are our priority, and our values are at the core of everything we do. Our dynamic and flexible environment encourages our teams to experiment, take ownership of decisions, and question convention to solve complex problems. We value shared wins, perseverance, and a growth mindset, which drives us forward, together.  

Among the things you'll discover at Alector from your very first day are our committed and driven colleagues, a bold company vision, and new, modern offices designed to inspire innovation and collaboration in South San Francisco, right at the heart of Biotech Bay. Our benefits are thoughtfully designed around Alectorians and their loved ones and include flexible hybrid work options, competitive compensation, and comprehensive and unique benefits that enhance your health and well-being. Come join us! 
 
We believe that hard-working teams include people from a wide variety of backgrounds and experiences who can challenge each other’s assumptions with fresh perspectives and bring creative ideas to the table. We are committed to building an open, diverse, and inclusive environment for all employees. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, sexual orientation, age, marital status, veteran status, or disability status, or any other characteristics protected under applicable federal, state, or local laws.  

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation. 

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About Alector

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

201 - 500 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2013

Social media

Twitter

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