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Gcp Qa Jobs (NOW HIRING)

Argenx

OR · On-site

$152K - $209K/yr

Provide QA input during the creation/revision of argenx clinical procedural documents for GCP compliance * When assigned as "QA Approver" in ARGO or PhoeniQS, act as QA approver for GCP area. * Act ...

Vrtx

GCP Quality Associate Director

Boston, MA · Hybrid

$160K - $240K/yr

The Associate Director, GCPComplianceis responsible forthe quality assurance and compliance ... Manage orassistin (internal and external) GCP Quality Events including, but not limited to ...

New

Exelixis

GCP/GVP QA Director

Alameda, CA

$185K - $263K/yr

The GCP/GVP QA Director is accountable for Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP) systems and activities, drives compliance and continuous improvement, ensures that ...

Exelixis

GCP/GVP QA Director

Alameda, CA · On-site

$185K - $263K/yr

The GCP/GVP QA Director is accountable for Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP) systems and activities, drives compliance and continuous improvement, ensures that ...

Exelixis

GCP/GVP QA Director

Alameda, CA

$185K - $263K/yr

The GCP/GVP QA Director is accountable for Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP) systems and activities, drives compliance and continuous improvement, ensures that ...

Novartis

Associate Director, Clinical QA

East Hanover, NJ · On-site +1

$158K - $237K/yr

Provide GCP guidance to day-to-day questions arising from Clinical trials deliverables. * Collaborate with Country Development QA and ESP QA to drive initiatives relevant to internal monitoring and ...

Exelixis

Senior GCP/PV/GLP QA Manager

Alameda, CA

$163K - $231K/yr

The Senior GCP/GVP QA Manager is accountable for assisting with the development, implementation and maintenance of end-to-end QA systems and activities for GCP/GLP operations, including planning and ...

Exelixis

Senior GCP/PV/GLP QA Manager

Alameda, CA · On-site

$163K - $231K/yr

The Senior GCP/GVP QA Manager is accountable for assisting with the development, implementation and maintenance of end-to-end QA systems and activities for GCP/GLP operations, including planning and ...

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How much do gcp qa jobs pay per year?

As of Jun 14, 2026, the average yearly pay for 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 GCP QA job?

A GCP QA (Good Clinical Practice Quality Assurance) job involves ensuring compliance with regulatory guidelines in clinical research. Professionals in this role conduct audits, review protocols, and ensure clinical trials adhere to industry standards such as FDA and ICH guidelines. They work to identify, report, and mitigate risks to maintain the integrity of clinical data. GCP QA specialists collaborate with regulatory agencies, clinical teams, and sponsors to ensure ethical and quality-driven research practices.

What are the key skills and qualifications needed to thrive in the Gcp Qa position, and why are they important?

To thrive as a GCP QA, you need a strong understanding of Good Clinical Practice (GCP) guidelines, clinical research processes, and quality assurance methodologies, often backed by a degree in life sciences or a related field. Experience with audit tools, electronic data capture (EDC), and certifications such as RQAP-GCP or similar are highly advantageous. Excellent attention to detail, communication skills, and the ability to work collaboratively stand out as essential soft skills. These capabilities ensure compliance, data integrity, and the smooth execution of clinical trials within regulatory frameworks.

What are some of the typical responsibilities of a GCP QA throughout a clinical trial?

GCP QA professionals are responsible for planning, conducting, and documenting quality audits of clinical trial processes, ensuring compliance with Good Clinical Practice guidelines and regulatory requirements. They review study documentation, identify compliance gaps, and work closely with clinical project teams to implement corrective actions. GCP QA specialists regularly communicate with sponsors, investigators, and regulatory agencies. Their oversight ensures data integrity and subject safety throughout the clinical trial lifecycle, which is vital for successfully bringing new therapies to market.

More about Gcp Qa jobs
What cities are hiring for Gcp Qa jobs? Cities with the most Gcp Qa job openings:
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Gcp Qa jobs near you
Infographic showing various Gcp Qa job openings in the United States as of June 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 78% Physical, 7% Hybrid, and 15% Remote job distribution, with an average salary of $118,074 per year, or $56.8 per hour.
Associate Director, Clinical Quality Assurance

Associate Director, Clinical Quality Assurance

Revolution Medicines

Redwood City, CA • Hybrid

$44.75 - $59.75/hr

Other

Posted 9 days ago

Job description

The Opportunity:

Revolution Medicines is seeking an Associate Director, Clinical Quality Assurance, who will play a key role within Quality Assurance and is responsible for providing leadership and compliance support for RevMed sponsored clinical trials with respect to RevMed's Standard Operating Procedures, applicable regulatory requirements (FDA, EU, ICH & country-specific), and current industry standards and practices.

  • Support the development and maintenance of applicable Quality Systems and procedures that comply with applicable GCP standards and guidelines.

  • Collaborate with clinical functions (e.g., Clinical Operations, Clinical Development) to provide GCP compliance support.

  • Participate in clinical study execution teams (CSETs) to enable risk-based quality management and a culture of quality and open dialogue.

  • Perform quality review of clinical trial documents with a focus on compliance / regulatory requirements and risk management.

  • Collaborate with internal stakeholders, external auditors, and auditees to support the planning, preparation, conduct, reporting, and closure of GCP audits.

  • Provide risk-based quality oversight for clinical trial activities and perform routine clinical vendor assessments.

  • Provide support for Inspection Readiness activities (e.g., TMF activities, study documentation).

  • Assess and coordinate activities relevant to potential quality issues associated with GCP and clinical trial conduct including but not limited to investigations, and root cause analysis, CAPA planning and management.

  • Escalate identified issues to QA Management and other relevant leadership as needed in a timely manner.

  • Enable other assigned GCP or GXP related tasks, as appropriate.

  • Support GCP audits and inspections of RevMed, Vendors, and clinical investigator sites by regulatory authorities or business partners.

  • Build positive professional relationships and trust to support learning, respect, open communication, collaboration, and teamwork.

Required Skills, Experience and Education:

  • Bachelor's degree in scientific or technical discipline.

  • A minimum of 10+ years of experience in GCP Quality in the pharmaceutical or biotechnology industry.

  • 8 years in any of the following areas: audit or audit management experience, inspection readiness, Deviation/CAPA management, or related quality management system responsibilities.

  • Extensive knowledge of ICH GCP, other relevant ICH guidelines and regulatory requirements (minimally US FDA) regarding applicable drug development regulations.

  • Effective communication (verbal and written).

  • Ability to build and sustain positive relationships with GxP colleagues, internal stakeholders, and external partners.

  • Ability to create innovative solutions to problems, while integrating stakeholder input and feedback.

  • Ability to critically evaluate and troubleshoot complex problems with diligence.

  • Ability to manage multiple priorities and aggressive timelines.

  • Highly responsible, self-motivated professional with enthusiasm and passion for the work.

  • Highly proficient with various Microsoft and other computerized systems (e.g., Word, Outlook, Excel, PowerPoint, Visio, etc.).

Preferred Skills:

  • Good knowledge of Computer System Validation. 

    #LI-Hybrid #LI-JC1

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