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Contract Gcp Qa Jobs (NOW HIRING)

WEP Clinical

Clinical Quality Assurance Manager

The Clinical Quality Assurance Manager is responsible for the strategic leadership, oversight, and ... Provide cross-functional oversight of the GCP Quality Management System to ensure compliance with ...

WEP Clinical

Clinical Quality Assurance Manager

The Clinical Quality Assurance Manager is responsible for the strategic leadership, oversight, and ... Provide cross-functional oversight of the GCP Quality Management System to ensure compliance with ...

Vrtx

Senior Manager, Clinical Study Quality Lead

Boston, MA · Hybrid

$137K - $206K/yr

This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support ...

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Contract Gcp Qa information

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How much do contract gcp qa jobs pay per year?

As of Aug 20, 2026, the average yearly pay for contract gcp qa in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

What is a contract GCP QA?

Contract GCP QA professionals are quality assurance specialists who work on a contractual basis to ensure that clinical trials comply with Good Clinical Practice (GCP) guidelines. They conduct audits, review documentation, and provide oversight to verify that all processes adhere to regulatory standards. Their role is crucial in maintaining the integrity and reliability of clinical research data, and they often work with multiple organizations or projects depending on the needs of the client. These professionals bring expertise in GCP regulations, clinical trial processes, and risk management.

What are the key skills and qualifications needed to thrive as a contract GCP QA?

To excel as a Contract GCP QA (Good Clinical Practice Quality Assurance), you need a solid understanding of clinical research processes, regulatory compliance, and GCP guidelines, often supported by a science degree and relevant QA experience. Familiarity with audit management tools, electronic trial master files (eTMF), and certifications such as RQA or ASQ are typically required. Strong attention to detail, analytical thinking, and effective communication skills help you identify issues and collaborate with clinical teams. These skills are vital to ensure clinical trials meet regulatory standards, safeguard data integrity, and support successful study outcomes.

What are some common challenges faced by a contract GCP QA, and how can they be effectively addressed?

As a Contract GCP QA (Good Clinical Practice Quality Assurance) professional, common challenges include staying updated with evolving regulatory requirements, adapting quickly to diverse client processes, and ensuring consistent quality across multiple clinical trials. Working on a contract basis often means rapidly acclimating to new teams and project scopes. To address these challenges, it’s important to maintain strong communication skills, actively seek clarification on project expectations, and regularly participate in training or professional development to stay current with industry standards.

What is the difference between Contract Gcp Qa vs Contract Gcp Developer?

AspectContract Gcp QaContract Gcp Developer
CertificationsGCP certifications, QA certificationsGCP certifications, development certifications
Work EnvironmentTesting environments, quality assurance teamsDevelopment environments, coding teams
Employer UsageTech companies, QA service providersTech companies, software development firms
Common Search IntentQA roles, testing, quality assuranceDevelopment roles, coding, software creation

Contract Gcp Qa focuses on testing, quality assurance, and ensuring GCP-based solutions meet standards. Contract Gcp Developer involves building, coding, and deploying applications on GCP. While both roles require GCP knowledge, QA emphasizes testing processes, whereas developers focus on creating and maintaining software.

What are the most commonly searched types of Gcp Qa jobs?

The most popular types of Gcp Qa jobs are:

What job categories do people searching Contract Gcp Qa jobs look for?

The top searched job categories for Contract Gcp Qa jobs are:

Contract Gcp Qa jobs near you
Infographic showing various Contract Gcp Qa job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 4% Part Time, 6% Contract, and 1% Nights. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $118,074 per year, or $56.8 per hour.

Director - Quality GCP

Monte Rosa Therapeutics, Inc

Boston, MA • On-site

$185K - $235K/yr

Full-time

Re-posted 5 hours ago

Job description

Overview
Monte Rosa Therapeutics is seeking a Director Quality GCP to provide strategic oversight of phase-appropriate Quality GCP and GCLP activities, including GCP quality oversight of ongoing quality activities supporting active pre-clinical and clinical programs through participation on in-house and external cross-functional teams. This role requires an 75% on-site presence. You will work closely with industry leaders in Boston and Basel . Join a diverse, collaborative, and dynamic team that values innovation, teamwork, and a people-centric culture!
Responsibilities
  • Primary GCP Quality contact for identified vendors and investigator sites supporting clinical programs as well as other GCP quality events (e.g., potential serious breach assessments, CAPAs)
  • Author key GCP quality SOPs and key reviewer for other quality (GxP) procedures.
  • Develop a risk-based GCP compliance program.
  • Support teams in the initiation, review, and closure of quality events and associated CAPA, Change Action, and Effectiveness plans.
  • Develop and provide GCP and other GxP training (as applicable).
  • Ensure appropriate qualification of vendors and ensure compliant vendor management and regular assessment/audits. May conduct GCP audits (vendors and sites).
  • Ensure audit observations are communicated, tracked and remediated.
  • Provide QA GCP review and feedback on regulatory submissions.
  • Lead and participate in inspection readiness activities for regulatory inspections - both internally and at clinical sites.
  • Interface with internal departments and external vendors on a variety of technical/quality subjects.

Qualifications
  • BS Degree in Chemistry, Pharmacy, Biology or a related life science, or a combination of a BS Degree with relevant Quality and Technical experience.
  • Minimum of 16 years of experience within the pharmaceutical or biopharmaceutical industry, with development experience and exposure to commercial operations.
  • Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus.
  • Able to provide solution-minded approach and flexibility to emerging challenges.
  • Able to appropriately balance priorities plus multi-task against competing priorities.
  • Proven experience with the desire, and ability to work in a fast-paced, matrixed, start-up environment.
  • Hands-on leader, able to provide solution-minded approach and flexibility to emerging challenges
  • Understanding of drug development and program management preferred.

Apply