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MSD

Senior Bioanalytical Associate

Gaithersburg, MD · On-site

$67K - $101K/yr

Training in and experience with GLP and/or GCLP is preferred * Experience with running immunoassays/ligand-binding assays is preferred * Experience with running assays on the MSD platform is ...

MSD

Associate Scientist, Bioanalytical Lab

Gaithersburg, MD · On-site

$78K - $116K/yr

Training in and experience with GLP and/or GCLP is highly preferred * Experience working in a high complexity/high throughput lab is highly preferred KNOWLEDGE, SKILLS AND ABILITIES: * Understanding ...

MSD

Bioanalytical Scientist

Gaithersburg, MD · On-site

Adhere to principles of GLP/GCLP applicable to bioanalytical sample testing, data analysis and reporting * Adhere to all laboratory safety policies and procedures including proper use of all required ...

Artech Information System LLC

Scientist

Groton, CT

... GCLP environment. In addition to running clinical samples, will also be involved for biomarker assay development and mechanistic studies. Ability to work occasional weekends for clinical sample ...

MSD

Sample Management Technician II

Gaithersburg, MD · On-site

$45K - $66K/yr

KNOWLEDGE, SKILLS AND ABILITIES • Knowledge of Good Laboratory Practice/Good Clinical Laboratory Practice (GLP/GCLP) • Strong proficiency in working with computers and Microsoft office ...

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How much do gclp jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for gclp in the United States is $24.06, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $25.96 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Good Clinical Laboratory Practice (GCLP) professional?

To thrive as a GCLP professional, you need a solid background in clinical laboratory sciences, regulatory compliance, and quality management, often supported by relevant degrees or certifications in laboratory practices. Familiarity with laboratory information management systems (LIMS), GCLP guidelines, and audit procedures is typically required. Attention to detail, strong organizational abilities, and effective communication are important soft skills for success in this role. These competencies ensure the accuracy, reliability, and regulatory compliance of laboratory data in clinical trials, which are critical for patient safety and valid research outcomes.

What is the difference between Gclp vs Clinical Laboratory Scientist?

AspectGclpClinical Laboratory Scientist
CertificationsGCLP certification, Good Clinical Laboratory PracticeASCP certification, CLS license
Work EnvironmentClinical research labs, pharmaceutical settingsHospital labs, diagnostic labs
Industry UsagePharmaceuticals, clinical researchHealthcare, diagnostics

Gclp professionals focus on ensuring compliance with Good Clinical Laboratory Practice in research settings, while Clinical Laboratory Scientists perform diagnostic testing in healthcare labs. Both roles require laboratory skills but differ in industry focus and certifications.

What is a GCLP professional?

GCLP professionals are individuals who work in compliance with Good Clinical Laboratory Practice (GCLP) standards. These standards ensure the quality, reliability, and integrity of laboratory data generated in clinical trials. GCLP professionals are responsible for overseeing laboratory operations, maintaining documentation, ensuring regulatory compliance, and supporting clinical research activities. Their work is critical in providing accurate laboratory results that support drug development and patient safety.

What are some common challenges faced by professionals working in a GCLP role, and how can they be addressed?

Professionals in a GCLP role often encounter challenges such as maintaining stringent compliance with regulatory standards, managing documentation accurately, and ensuring effective communication between laboratory and clinical teams. Adapting to evolving guidelines and integrating new technologies can also present difficulties. Addressing these challenges involves ongoing training, robust quality management systems, and fostering a culture of open collaboration, which helps ensure data integrity and smooth workflow in clinical research settings.
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Gclp jobs near you
Infographic showing various Gclp job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $50,049 per year, or $24.1 per hour.

Scientist I, Bioanalytical

Maze Therapeutics

South San Francisco, CA • Hybrid

Other

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago

Job description

The Position

We are seeking a detail-oriented Scientist to work in the Non-Clinical Development department overseeing bioanalytical work for Maze. In this role, you will oversee bioanalysis for Good Laboratory Practices (GLP), Good Clinical Laboratory Practices (GCLP), and non-GLP studies in support of the development of small molecule drugs. As part of the Non-Clinical Development team, you will have the opportunity to contribute to key drug discovery and development projects. 

This position reports to VP, Non-Clinical Development. 

The Impact You'll Have
  • Oversee the development, validation, and execution of bioanalytical assays for both pharmacokinetics and pharmacodynamics for ongoing preclinical, nonclinical, and clinical programs. 
  • Manage the collaborations with contractor laboratories conducting bioanalysis and review data from analysis to confirm analyses were correctly conducted and batch analyses met acceptance criteria. 
  • Provide written summaries of bioanalytical methods for regulatory submissions as needed. 
  • Coordinate regulated bioanalysis activities across development programs, ensuring compliance with timelines and regulatory standards. 
  • Provide timeline updates to the Head of Bioanalysis, Nonclinical Development, and collaborate with key stakeholders in Research, Regulatory Affairs, Manufacturing, Quality, and Clinical Sciences to address bioanalysis-related project issues. 
  • Review, investigate, and coordinate resolution of study queries with contract research organization (CRO) and personnel regarding data integrity. 
What We're Looking For
  • Bachelor's degree in analytical chemistry, chemistry, biochemistry, or related field. 
  • 6+ years of relevant experience, ideally within a pharmaceutical company, a CRO, or academia, with a focus on bioanalysis oversight. 
  • Experience and understanding of GLP and GCLP principles and guidances 
  • Experience in GLP and GCLP analysis of one or more bioanalytical techniques, including: LC-MS/MS, ELISA, and MSD 
  • Experience working with multidisciplinary project teams, driving successful outcomes. 
  • Ability to manage multiple projects simultaneously with excellent attention to detail. 
  • Clear and effective communication skills to present complex scientific information to various stakeholders. 
About Maze Therapeutics

Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing human genetics to develop precision medicines for patients with kidney and metabolic diseases. Our clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease. We are also advancing a preclinical pipeline through our Compass platform, which links human genetic variants to the biological pathways that drive disease.

Our People

Maze is comprised of a team of passionate and creative professionals committed to discovering and delivering transformative medicines to patients suffering from both rare and common genetic diseases. We are fostering a culture that encourages vision, initiative and the development of talent. Our supportive work environment inspires creative thinking and freedom of expression, resulting in a stimulating atmosphere where people enjoy coming to work. While we have a passion for advanced science and pride ourselves on excellence in execution, ultimately, everything we do is about patients. 

Our Core Values

Further Together - Our path is paved with challenges, but with resilience and a team-first mentality, we'll achieve our mission. 

Impact Obsessed - We embrace the bold, take calculated risks, and learn from our mistakes to improve the lives of others.

Stand True - Our integrity is foundational; it guides us no matter the obstacle.

The expected annual salary range for employees located in the San Francisco Bay Area is $130,000 - $159,000. Additionally, this position is eligible for an annual performance bonus.

Maze performs position-based compensation benchmarking to industry market data to ensure we pay competitive wages. Determination of starting salary will depend upon a variety of job-related factors, which may include professional experience, skills, and job location. The expected salary range for this role may be modified in the future.

Maze offers a robust benefits package to our eligible employees including competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with employer match and a generous holiday and PTO policy.

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