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Glp Project Manager Jobs (NOW HIRING)

Understanding of ICH, GCP, GLP, and local regulations * LabMatrix experience preferred * Strong ... Project Management experience is also preferred. * Very high attention to detail and excellent ...

Job Summary The Biospecimen Project Manager will be the centralized point of contact developing and ... Understanding of ICH, GCP, GLP, and local regulations required * Ability to draft SOPs, work ...

The Lab QMS Project Manager will provide project leadership, coordination, and oversight for ... 9001, CLIA, CAP, GLP, FDA quality requirements, CDC policies, and other program-specific ...

Excellent organizational and project management abilities. * Strong negotiation, influencing, and ... GLP/GCP Lead Internal Auditor and take your career to the next level at Labcorp. Imagine being ...

Excellent organizational and project management abilities. * Strong negotiation, influencing, and ... GLP/GCP Lead Internal Auditor and take your career to the next level at Labcorp. Imagine being ...

The Project Manager will report to the Project Executive and partner with Engineering, QA ... GMP/GLP labs, ISO 14644 cleanrooms, ISO 17025 laboratories, or similar. * Experience working on ...

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Glp Project Manager information

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$38.5K

$102.7K

$162K

How much do glp project manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for glp project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

What is a GLP Project Manager?

GLP Project Managers are professionals responsible for overseeing projects that must comply with Good Laboratory Practice (GLP) regulations. They manage the planning, execution, and documentation of studies to ensure all processes meet regulatory standards and guidelines. Their role involves coordinating teams, maintaining quality assurance, and ensuring all data generated is reliable and traceable for regulatory submissions. GLP Project Managers often work in pharmaceutical, biotechnology, or contract research organizations.

How does a GLP Project Manager typically collaborate with laboratory staff and regulatory teams during a study?

A GLP Project Manager acts as a central point of communication between laboratory staff, regulatory affairs, and sometimes clients to ensure that studies comply with Good Laboratory Practice (GLP) standards. They coordinate project timelines, clarify regulatory requirements, and resolve any issues that arise during the study process. Regular meetings, detailed documentation, and clear delegation of tasks help facilitate smooth collaboration. This role often requires balancing strict regulatory compliance with the practical needs of scientific teams, making strong interpersonal and organizational skills essential.

What are the key skills and qualifications needed to thrive as a GLP Project Manager, and why are they important?

To thrive as a GLP Project Manager, you need a comprehensive understanding of Good Laboratory Practice (GLP) regulations, project management methodologies, and a background in life sciences or related fields. Familiarity with project management software (such as MS Project), laboratory information management systems (LIMS), and relevant GLP certifications is often required. Exceptional organizational, leadership, and communication skills help coordinate multidisciplinary teams and ensure regulatory compliance. These skills and qualifications are essential to successfully manage complex studies, meet regulatory standards, and deliver high-quality results on time and within scope.

What are popular job titles related to Glp Project Manager jobs?

For Glp Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Glp Project Manager job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, 11% Hybrid, and 22% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Senior Biospecimen Project Manager

Remote

labconnect
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees

Full-time

Re-posted yesterday


Job description


The Senior Biospecimen Project Manager will be the centralized point of contact to drive biospecimen lifecycle management and resulting analytical data from clinical studies.

Please note: This is a remote role is open to candidates based in the United States. Candidates located in California are eligible only if they reside outside of the San Francisco Bay Area (defined as locations more than 100 miles from the Bay Area).


Responsibilities:

  • Drive biospecimen lifecycle management from sample receipt to analysis and final disposition
  • Ensure accurate specimen metadata
  • Communicate study specimen updates to client groups and stakeholders
  • Increase the efficiency of specimen management through sharing of knowledge and best practices
  • Provide site support and drive query resolution
  • Participate or lead special projects as assigned
  • Adhere to client policies and Standard Operating Procedures
  • Review clinical study protocols and service providers’ scope of work documents
    for sample handling and processing details
  • Set up and maintain a complex study sample tracker – experience in manual sample tracking for complex clinical studies
  • Create and manage project plans
  • Manage data transfer plans with analytical laboratories
  • Manage data received from external and internal laboratories, including data generated in exploratory studies
  • Manage specimen metadata discrepancies and ensure resolution
  • Submit specimens for analytical assays per study timelines
  • Review status of specimens collected and completeness of data
  • Contribute to meeting database locks by ensuring all specimens have a final result and data transfer is complete; create reports for data management as needed
  • Provide guidance to others and act as technical resource within the department
  • Lead projections for annual and long-term planning to clinical team
  • Provide oversight and management to junior personnel

Skills/Abilities:

  • Understanding of transaction-based inventory and data management systems as well as clinical trial processes
  • Understanding of ICH, GCP, GLP, and local regulations
  • LabMatrix experience preferred
  • Strong excel experience required, extensive macro and template building knowledge desired
  • Strong computer literacy, including Word, SharePoint, Smartsheet and PowerPointAdvanced planning, organizational, time management skills


Experience / Education:

  • B.A./B.S. in life sciences, medical technology, or related field and 5-7 years of directly related experience.
  • Experience in life sciences or medically related fields, including clinical development, biospecimen lifecycle management, or clinical laboratory analysis.
  • Project Management experience is also preferred.
  • Very high attention to detail and excellent multi-tasking skills is required for success in this position.