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Gclp Jobs (NOW HIRING)

Artech Information System LLC

Bench Scientist

Cambridge, MA · On-site

$38.50 - $48.25/hr

Scientist BS with 5+ year, MS with 2+ years experienced scientist to run flow cytometry clinical samples in a GCLP environment. In addition to running clinical samples , will also be involved for ...

Artech Information System LLC

Scientist

Groton, CT · On-site

Scientist BS with 5+ year, MS with 2+ years experienced scientist to run flow cytometry clinical samples in a GCLP environment. * In addition to running clinical samples, will also be involved for ...

MSD

Senior Study Coordinator

Gaithersburg, MD · On-site

$67K - $101K/yr

... GCLP), with minimal supervision. This includes, but is not limited to, project related support by creating study-specific documentation, assisting the Bioanalytical Principal Investigators (BPIs) in ...

Kelly Services

Quality Assurance Manager

Pleasanton, CA

$175K - $200K/yr

Establish and ensure compliance with GLP, GCLP, and applicable FDA and international regulatory standards. * Develop and manage the company's Master Schedule. * Create, administer, and maintain QA ...

Kelly Services

Quality Assurance Manager

Pleasanton, CA

$175K - $200K/yr

Establish and ensure compliance with GLP, GCLP, and applicable FDA and international regulatory standards. * Develop and manage the company's Master Schedule. * Create, administer, and maintain QA ...

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How much do gclp jobs pay per hour?

As of Jun 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, and why are they important?

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 job makes $10,000 a month without a degree?

A GCLP (Good Clinical Laboratory Practice) professional in the biotech or pharmaceutical industry can potentially earn $10,000 or more per month through roles such as senior laboratory managers or clinical research coordinators, especially with extensive experience and certifications. These positions often require specialized knowledge of laboratory standards, regulatory compliance, and strong technical skills, but may not require a traditional college degree.

What are GCLP professionals?

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 (Good Clinical Laboratory Practice) 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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What job categories do people searching Gclp jobs look for? The top searched job categories for Gclp jobs are:
Gclp jobs near you
Infographic showing various Gclp job openings in the United States as of May 2026, with employment types broken down into 98% Full Time, 1% Part Time, and 1% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $50,049 per year, or $24.1 per hour.
Manager/ Director of Quality Assurance

Manager/ Director of Quality Assurance

CRYSTAL PHARMATECH INC

Pleasanton, CA • On-site

$120K - $180K/yr

Full-time

Medical, Dental, Retirement, PTO

Posted 29 days ago

Job description

Benefits:
  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Paid time off
  • Parental leave
  • Wellness resources

Company Description
Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading biologics analytical organization with operations in the San Francisco Bay Area and New Jersey. We specialize in bioanalytical and CMC analytical services for biotech and pharmaceutical companies developing biologics. Our expertise spans a wide range of therapeutic modalities, supporting projects from discovery through clinical development.
Role Description
Reporting directly to the CEO, the Director of Quality Assurance (QA) will be responsible for the development, management, and continuous improvement of quality systems ensuring compliance with Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), and other applicable regulatory standards for our bioanalytical GLP lab in Pleasanton, California. This role ensures that facilities, equipment, personnel, and procedures meet all regulatory requirements and effectively supports nonclinical and clinical testing activities.
Key Responsibilities
  • Host client and regulatory inspections, including preparing and submitting responses to findings.
  • Support regulatory activities across all BABM sites within the organization.
  • Audit raw data, summary tables, and reports associated with GLP and GCLP protocols to ensure compliance with regulatory requirements.
  • Maintain inspection readiness, including preparing and managing site-specific documentation.
  • Establish and ensure compliance with GLP, GCLP, and applicable FDA and international regulatory standards.
  • Develop and manage the companys Master Schedule.
  • Create, administer, and maintain QA Standard Operating Procedures (SOPs), QA files, and QA audit logs.
  • Process, archive, and maintain QA department inspection reports and supporting documentation.
  • Monitor and interpret regulatory requirements to ensure alignment with business processes and procedures.
  • Author and review SOPs and Statistical Analysis Plans (SAPs).
  • Provide GLP and GCLP training to staff.
  • Recruit, develop, and mentor QA professionals, fostering a culture of growth and excellence.
  • Conduct and report inspections of internal facilities and audits of external vendors to assess compliance with regulatory standards.
  • Establish and administer a company Risk Register.
  • Identify and address regulatory compliance issues, providing guidance to other departments.
  • Deliver monthly compliance status reports to Test Site Management (TSM), highlighting issues and corrective actions.
  • Represent the QA function in company meetings.

Qualifications
  • Bachelors degree in biological, chemical, or physical sciences (required); advanced degrees (e.g., Masters, Ph.D.) preferred.
  • 10+ years of relevant regulatory affairs experience in the bioanalytical CRO or biotechnology/pharmaceutical industry, or a combination of education and experience.
  • Proven ability to provide regulatory leadership and guidance in cross-functional and matrixed environments.
  • Strategic thinker with strong planning skills and the ability to propose innovative solutions to regulatory challenges.

The salary range represents the anticipated base pay for this position. Actual compensation may vary based on factors including, but not limited to, skills, qualifications, experience, education, and location.
As part of our recruitment process, we may use technology-assisted tools to support application review and improve efficiency. All hiring decisions are made by our team.
Crystal Bio Solutions is an equal opportunity employer. We are committed to creating an inclusive environment for all employees and applicants and do not discriminate based on race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, or any other protected status in accordance with applicable laws.