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Commission Gcp Qa Jobs (NOW HIRING)

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site

$160 - $200/hr

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 ...

Shionogi Inc.

Senior Manager, GCP QA

Florham Park, NJ · On-site

$135 - $165/hr

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 ...

Shionogi Inc.

Senior Manager, GCP QA

Florham Park, NJ · On-site

$135K - $165K/yr

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 ...

Shionogi Inc.

Senior Manager, GCP QA

Florham Park, NJ · On-site

$135K - $165K/yr

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 ...

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site +1

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 ...

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site

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 ...

Shionogi Inc.

Senior Manager, GCP QA

Florham Park, NJ · 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 ...

Madrigal Pharmaceuticals

Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... Position Summary This position will be responsible for GCP/Clinical Quality Assurance activities.

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Commission Gcp Qa information

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How much do commission gcp qa jobs pay per hour?

As of Aug 20, 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?

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

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Commission Gcp Qa jobs near you
Infographic showing various Commission Gcp Qa job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 9% Part Time, and 5% Contract. Highlights an 57% Physical, 1% Hybrid, and 42% Remote job distribution, with an average salary of $97,144 per year, or $46.7 per hour.

Director, GCP Quality Assurance

Beeline Medicines

Boston, MA • Hybrid

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Summary:

The Director, GCP Quality Assurance is responsible for providing strategic and operational Quality Assurance oversight for Good Clinical Practice (GCP) activities supporting the company's clinical development programs. This role ensures that clinical trials are conducted in compliance with applicable regulatory requirements, company policies, and global GCP standards, with a continuous state of inspection readiness.

The Director partners closely with Clinical Operations, Regulatory Affairs, Pharmacovigilance, Data Management, and external service providers to implement a risk-based quality oversight model across the clinical lifecycle. The role is accountable for GCP quality systems, vendor oversight, audits, and inspection support, and plays a critical role in embedding quality by design into clinical development programs


Work Arrangement & Location: 

Hybrid - This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week - currently designated as Tuesday and Wednesday. Additional on-site days may be required based on business needs, team priorities, or leadership direction.


Essential Duties and Responsibilities:

  • Develop and implement the GCP QA strategy aligned with clinical development objectives and global regulatory expectations
  • Serve as a key QA partner to Clinical Operations and cross-functional stakeholders on GCP compliance and quality risk management.
  • Promote a strong culture of quality, compliance, and continuous improvement across clinical programs
  • Oversee GCP quality systems including deviations, investigations, CAPAs, change control, documentation, and training related to clinical activities.
  • Ensure GCP processes are phase-appropriate, compliant, and scalable
  • Support the development, review, and approval of GCP-related SOPs, policies, and work instructions.
  • Provide QA oversight for GCP activities conducted internally and by CROs, vendors, and other service providers
  • Lead GCP vendor qualification, audit strategy, and ongoing oversight using risk-based principles.
  • Review and approve GCP-related quality agreements and vendor oversight plans
  • Plan and execute risk-based GCP audits, including CRO audits, investigator site audits, and system audits as applicable.
  • Lead GCP inspection readiness activities and serve as a primary QA contact during health authority inspections.
  • Coordinate inspection preparation, conduct, and follow-up, including responses to regulatory observations.
  • Ensure a sustainable state of inspection readiness across clinical programs.
  • Ensure critical-to-quality considerations are embedded in clinical trial design and execution.
  • Provide oversight of data integrity practices across GCP processes and systems.
  • Identify, assess, and proactively mitigate GCP compliance risks
  • Perform other duties and responsibilities as assigned


Qualifications:

  • Education: Bachelor's degree in a scientific or related discipline; advanced degree preferred.
  • 10+ years of experience in GCP Quality Assurance or Clinical Quality within a biotech or pharmaceutical environment.
  • Strong knowledge of global GCP regulations and clinical trial oversight requirements.
  • Demonstrated experience supporting regulatory inspections and audits.
  • Experience overseeing CROs and other GCP service providers.
  • Experience supporting late-stage or pivotal clinical trials.
  • Strong background in risk-based quality management and inspection readiness.
  • Skilled at influencing without authority; effectively engages senior scientific, clinical, and operational stakeholders to drive alignment on quality priorities and shared accountability for compliance
  • Able to serve as a primary quality representative in regulatory agency interactions and inspections, communicating the company's quality posture with confidence and credibility.
  • Strong cross-functional collaborator who proactively communicates quality risk, escalates issues with appropriate context and urgency, and fosters a culture of transparent, solution-oriented dialogue.

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