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Commission Gcp Qa Jobs (NOW HIRING)

Senior Manager, GCP Quality Assurance page is loaded## Senior Manager, GCP Quality ... Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ...

Oversee GCP framework for sponsored clinical trials to ensure required quality elements are strategically executed upon, risk-based, as appropriate. * Oversee the clinical QA audit program, including ...

Senior Manager, GCP QA

Florham Park, NJ ยท On-site

$135K - $165K/yr

We are seeking an experienced Senior Manager, GCP QA to join our team. This role is crucial for ensuring quality oversight of clinical studies and vendor programs, maintaining compliance with ICH GCP ...

Overview We are seeking an experienced Senior Manager, GCP QA to join our team. This role is crucial for ensuring quality oversight of clinical studies and vendor programs, maintaining compliance ...

The Sr. Director, GCP Quality Assurance oversees the development, implementation, and maintenance of quality assurance systems and activities that support clinical trial quality, GCP compliance, and ...

Senior Manager, GCP QA

Florham Park, NJ ยท On-site

$135K - $165K/yr

We are seeking an experienced Senior Manager, GCP QA to join our team. This role is crucial for ensuring quality oversight of clinical studies and vendor programs, maintaining compliance with ICH GCP ...

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Commission Gcp Qa information

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How much do commission gcp qa jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for commission gcp qa in the United States is $46.70, according to ZipRecruiter salary data. Most workers in this role earn between $29.81 and $62.02 per hour, depending on experience, location, and employer.

What is a Commission GCP QA?

A Commission GCP QA (Good Clinical Practice Quality Assurance) is a professional responsible for ensuring that clinical trials and studies comply with regulatory guidelines, ethical standards, and GCP regulations. They conduct audits, review documentation, and assess processes to ensure data integrity and patient safety. The 'commission' aspect often refers to working on a contract or project basis rather than as a full-time employee. Their work is crucial in maintaining the credibility and reliability of clinical research data.

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

To thrive as a Commission GCP QA (Good Clinical Practice Quality Assurance), you need a solid background in clinical research, regulatory compliance, and GCP guidelines, typically supported by a life sciences degree and relevant QA experience. Familiarity with auditing tools, electronic trial master files (eTMF), and certifications such as RQAP-GCP or equivalent are commonly required. Strong attention to detail, analytical thinking, and effective communication skills are essential soft skills for this role. These competencies are crucial for ensuring that clinical trials adhere to regulatory standards, protect patient safety, and maintain data integrity.

What are some common challenges faced by a Commission GCP QA professional when ensuring compliance in complex clinical trials?

Commission GCP QA professionals often encounter challenges such as keeping up with evolving regulatory requirements, ensuring consistency in documentation across multiple trial sites, and managing communication between diverse teams. Navigating audits and inspections, particularly when trials are conducted internationally, can also be complex due to varying local regulations. Strong attention to detail, proactive problem-solving, and effective collaboration with clinical operations, data management, and regulatory affairs teams are essential to overcome these hurdles and maintain high compliance standards.

What is the difference between Commission Gcp Qa vs Cloud Quality Analyst?

AspectCommission Gcp QaCloud Quality Analyst
CertificationsGCP certifications, QA testing certificationsGCP certifications, QA testing certifications
Work EnvironmentCloud platforms, QA testing teamsCloud platforms, QA testing teams
Industry UsageTech companies using GCP for cloud solutionsTech companies focusing on cloud service quality
Primary FocusCommissioning and quality assurance of GCP projectsQuality assurance of cloud services and applications

Both roles involve quality assurance and GCP knowledge, but Commission Gcp Qa emphasizes commissioning processes within GCP projects, while Cloud Quality Analyst focuses broadly on cloud service quality across platforms. The roles often overlap but differ in scope and specific responsibilities.

What cities are hiring for Commission Gcp Qa jobs?

Cities with the most Commission Gcp Qa job openings:

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

The most popular types of Gcp Qa jobs are:

What states have the most Commission Gcp Qa jobs?

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Infographic showing various Commission Gcp Qa job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 83% Full Time, 9% Part Time, and 7% Contract. Highlights an 71% Physical, 1% Hybrid, and 28% Remote job distribution, with an average salary of $97,144 per year, or $46.7 per hour.

Director, GCP Quality Assurance

San Diego, CA โ€ข On-site

Scorpion Therapeutics
51 - 200 employees

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Position Summary

The Director, GCP Quality Assurance leads Good Clinical Practice (GCP) audit activities across the clinical development portfolio to ensure compliance with global regulatory requirements and internal quality standards. Provides strategic oversight of GCP quality systems, manages audit programs, supports inspection readiness, and serves as a GCP compliance subject matter expert.

Primary Responsibilities
  • Plan, schedule, conduct, and manage internal/external GCP audits of CSPs, CROs, investigator sites, and vendors
  • Prepare/review/finalize audit reports; document observations, risks, and corrective actions; track to resolution
  • Develop/review/maintain GCP Quality Agreements with CROs, CSPs, and clinical study partners
  • Maintain GCP audit metrics and deliver quality/compliance reporting for management reviews and continuous improvement
  • Develop/review/maintain SOPs and quality documents supporting GCP auditing and compliance
  • Manage internal GCP audit program (planning, execution, follow-up, and effectiveness assessments)
  • Support mock and regulatory inspections and responses for GCP studies/quality systems
  • Provide GCP compliance guidance to cross-functional stakeholders to ensure adherence to FDA, ICH, EU, and other global requirements
  • Recommend and implement improvements to GCP quality systems, processes, and procedures
Education & Experience (Required)
  • Bachelorโ€™s in Life Sciences or related field (or equivalent education/experience)
  • 10+ years in pharmaceutical/biotech/regulated industry
  • 5+ years in GCP Quality Assurance, compliance, and auditing
  • Lead Auditor experience for internal/external GCP audits
  • Strong knowledge of ICH-GCP and applicable FDA/EU/international GCP regulations
  • Audit experience covering CROs, investigator sites, and GCP service providers
  • Experience supporting regulatory inspections/inspection readiness
Preferred Qualifications
  • SQA/ASQ/Lead Auditor certification
  • Experience conducting global audits across US/EU/UK/Japan and other regions
  • Experience with eCOA, CSV, and data management
Benefits (as stated)
  • Medical, dental, vision; 401(k) match 1:1 up to 5%; equity; bonus; life/disability/EAP; tuition assistance; paid time off; paid parental leave; sick time.
Physical/Other
  • Ability to travel overnight independently and work after hours if required.
  • Occasionally lift/move up to 15 pounds.
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