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Clia Inspector Jobs in Boston, MA (NOW HIRING)

Quanterix

Senior Design Quality Engineer

Billerica, MA · Hybrid

$125K - $150K/yr

... and inspections. * Help to drive and foster a quality environment and mindset throughout the ... Our industry-leading precision instruments, digital immunoassay technology and CLIA-certified ...

QUEST DIAGNOSTICS INC

Lab Supervisor

Marlborough, MA · On-site

$95 - $125/hr

Adheres to all established CLIA, HIPAA, OSHA and laboratory safety requirements. * Required to use ... Participate in government or regulatory agency inspections, if needed. * Other duties as assigned.

Staffingine LLC

Lead Medical Technologist

Brighton, MA · On-site

$81K - $110K/yr

... and CLIA). Reviews applicable AABB Standards and CAP Checklists for departmental compliance and ... inspection. May be required to tabulate and report monthly transfusion data to National Health ...

Quest Diagnostics

Lab Supervisor

Marlborough, MA · On-site

$95K/yr

Adheres to all established CLIA, HIPAA, OSHA and laboratory safety requirements. * Required to use ... Participate in government or regulatory agency inspections, if needed. * Other duties as assigned.

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Showing results 21-40

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Clia Inspector information

What is a Clia inspector?

A CLIA Inspector is responsible for ensuring that clinical laboratories comply with the regulations set by the Clinical Laboratory Improvement Amendments (CLIA). They conduct inspections, review laboratory procedures, and assess compliance with federal standards for accuracy and reliability in patient testing. Inspectors may also provide guidance to labs on maintaining proper certification and improving quality control measures.

What are the key skills and qualifications needed to thrive as a Clia inspector?

To thrive as a CLIA Inspector, you need a comprehensive understanding of laboratory science, regulatory standards, and quality assurance procedures, typically supported by a degree in a related field and experience in clinical laboratory environments. Familiarity with CLIA regulations, laboratory information management systems (LIMS), and inspection protocols is essential. Strong attention to detail, analytical thinking, and effective communication are vital soft skills for this role. These skills and qualifications are crucial to ensure laboratories maintain compliance, uphold high-quality standards, and deliver accurate patient results.

What are the most common challenges faced by a Clia inspector in the field?

CLIA Inspectors often face the challenge of staying current with evolving regulations and ensuring diverse laboratories consistently meet complex compliance standards. They must adapt to varied laboratory environments, each with its own unique procedures and potential issues, while managing tight inspection schedules. Additionally, inspectors communicate findings and recommendations to laboratory staff, which requires both technical expertise and strong interpersonal skills. Overcoming these challenges contributes to maintaining healthcare quality and patient safety.

What are the most commonly searched types of Clia Inspector jobs in Boston, MA?

The most popular types of Clia Inspector jobs in Boston, MA are:

What are popular job titles related to Clia Inspector jobs in Boston, MA?

For Clia Inspector jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Clia Inspector jobs in Boston, MA look for?

The top searched job categories for Clia Inspector jobs in Boston, MA are:

Clia Inspector jobs near you
Infographic showing various Clia Inspector job openings in Boston, MA as of August 2026, with employment types broken down into 72% Full Time, 20% Part Time, 6% Contract, and 2% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Clinical Contract Coordinator II

CYNET SYSTEMS

Cambridge, MA • On-site

$37 - $42/hr

Contractor

Re-posted 11 days ago

Job description

Job Overview:

Pay Range: $37.81hr - $42.81hr

Requirement/Must Have:

  • 3+ years of professional experience in biospecimen management, clinical laboratory operations managing biospecimens in clinical trials or research settings.
  • Bachelor’s degree required in Biological Sciences, Biomedical Sciences, Biotechnology, Clinical Laboratory Science, Public Health and Life Sciences or related field.

Responsibilities:

  • Organize the biological specimen management laboratory, including the reception, registration, storage, and shipment of biospecimens.
  • Ensure compliance with regulatory requirements, quality standards, and ethical guidelines while managing biospecimen operations across multiple studies and sites.
  • Coordinate and manage laboratory sample operations, ensuring accurate receipt, processing, storage, and tracking of biological specimens.
  • Receive, record, store, dispose of, and ship biospecimens addressed to the laboratory from across global locations and verify the compliance of the related delivery documentation.
  • Perform the registration of pre-clinical/clinical study biospecimens received in LIMS (Laboratory Information Management System e.g., Watson) and generate and send documents related to these receptions.
  • Manage the recording of receptions and shipments in dedicated tracking files.
  • Detect, analyze, and report inconsistencies during biospecimen reception and registration.
  • Ensure the creation of study designs in Watson LIMS.
  • Ensure the maintenance of the laboratory work areas and proper functioning of equipment.
  • Monitor regular equipment maintenance and update established documentation.
  • Ensure and perform registration and update of inventories (biospecimen, equipment, and consumables).
  • Continuously participate in improving the department's operations and ensure that safety instructions are followed.
  • Create and/or update procedures.
  • Participate in meetings and working groups, propose technical, organizational, and documentary improvements, and participate in process optimizations.
  • Support audits and inspections; act as spokesperson for sample-related processes and documentation.
  • Implement translational medicine and biospecimen management strategies aligned with clinical development objectives.
  • Partner with clinical study teams to integrate biospecimen requirements into study protocols.
  • Collaborate with translational medicine and biomarker teams on biospecimen utilization.
  • Review study documents such as the protocol, Informed Consent Form, central laboratory specifications, electronic Case Report Form (eCRF) Specifications, Data collection strategy, etc.
  • Lead the design and optimization of biospecimen collection protocols and workflows.
  • Create the Biospecimen Management Plan (SMP) containing instructions for collection, storage, and shipping of biospecimens.
  • Manage relationships with the bioanalysis outsourcing, central laboratories, biorepositories, and third-party vendors as needed.
  • Ensure proper chain of custody, tracking, and inventory management of all biospecimens.
  • Create reports containing biospecimen statuses and perform overall monitoring of these biospecimens, from collection to destruction.
  • Ensure the traceability of associated documentation in the electronic Trial Master File (eTMF).

Skills:

  • Biospecimen management and lab coordination expertise.
  • Strong biospecimen lifecycle expertise.
  • Clinical trial systems and tools experience.
  • LIMS (e.g., Watson) proficiency.
  • Excellent cross-functional coordination skills.
  • Knowledge of regulatory requirements (GCP, GCLP, CLIA, CAP) and quality standards.
  • Proficiency with Laboratory Information Management Systems (LIMS) and specimen tracking platforms.
  • Experience with clinical trial sample management.
  • Knowledge of ICH-GCP guidelines and regulatory requirements.
  • Familiarity with clinical trial management and electronic data capture (EDC) systems.
  • Flexibility to support urgent sample processing needs.
  • Strong communication and team management capabilities.
 

Founded in 2010 and headquartered in the Washington, DC metro area, Cynet Systems Inc. is a leading staffing and recruiting powerhouse. Proudly recognized as a nationally and locally certified diversity firm, Cynet delivers agile, scalable talent solutions across industries. With an active footprint in all 50 U.S. states and Canada, we support thousands of consultants through our expansive, high-performing recruitment engine operating across North America and Asia—ensuring speed, quality, and consistency in every hire.
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About Cynet Systems

Sourced by ZipRecruiter

Cynet Systems Inc is a staffing and recruiting corporation nestled in Ashburn, VA, USA. Established in 2010, the company operates within the Information Technology and Services sector, specializing in providing effective workforce solutions to different business needs, including IT consulting, direct hire, and contract staffing services. Through the years, Cynet Systems has built an impressive portfolio, going beyond borders and expanding its operations internationally in Canada and India. Rooted in its core values of teamwork, leadership, and commitment, Cynet Systems helps businesses unlock their full potential by providing versatile and competent professionals that perfectly align with their needs. Fueled by their unwavering mission to deliver top-tier talent to businesses worldwide, Cynet Systems garnered various recognitions including SIA's fastest-growing staffing firms and Best Place to Work in Virginia for 2019.

Industry

It services

Company size

501 - 1,000 Employees

Headquarters location

Sterling, VA, US

Year founded

2010

Social media

Twitter

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