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Contract Gcp Auditor Jobs (NOW HIRING)

Alkermes

Manager, Clinical Quality Assurance

Waltham, MA · On-site +1

$135K - $149K/yr

Clinical auditing and/or compliance experience for relevant GCP or GVP related fields. With ... Work with contract auditors and CQA management to develop study specific audit plans * Review and ...

Madrigal Pharmaceuticals

Review CDAs, MSAs or contract/Work Orders * Conduct or manage internal/external audits (clinical ... include auditing of clinical trial vendors, sites and/or TMFs or internal R&D process audits

Sobi

QA Manager, GCP

San Diego, CA · On-site

$112K - $153K/yr

... provisions in contracts/Quality agreements, as applicable * QA representative during GCP ... Documented education/experience in QA systems and preferably auditing Soft skills: * Structured ...

Sobi

QA Manager, GCP

San Diego, CA · On-site

$112K - $153K/yr

... provisions in contracts/Quality agreements, as applicable * QA representative during GCP ... Documented education/experience in QA systems and preferably auditing Soft skills: * Structured ...

Sobi

QA Manager, GCP

San Diego, CA

$112K - $153K/yr

... provisions in contracts/Quality agreements, as applicable * QA representative during GCP ... Documented education/experience in QA systems and preferably auditing Soft skills: * Structured ...

Sobi

QA Manager, GCP

San Diego, CA · On-site

... provisions in contracts/Quality agreements, as applicable * QA representative during GCP ... Documented education/experience in QA systems and preferably auditing Soft skills: * Structured ...

Sobi

QA Manager, GCP

San Diego, CA · On-site

$112K - $153K/yr

... provisions in contracts/Quality agreements, as applicable * QA representative during GCP ... Documented education/experience in QA systems and preferably auditing Soft skills: * Structured ...

IQVIA, Inc.

Senior QA Auditor - GCP Audits

Durham, NC · On-site

$75K - $188K/yr

... with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer ... GCP experience. Equivalent combination of education, training and experience. * Experienced in the ...

IQVIA

Senior QA Auditor - GCP Audits

Durham, NC · On-site

$75K - $188K/yr

... with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer ... GCP experience. Equivalent combination of education, training and experience. * Experienced in the ...

Alkermes

Associate Director, Clinical QA

Waltham, MA · On-site

$166K - $181K/yr

Work with contract auditors and CQA management to develop study specific audit plans * Review and ... Plan and conduct GLP, GCP clinical vendor audits * When indicated collaborate with Clinical ...

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Contract Gcp Auditor information

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$38.5K

$92.8K

$151K

How much do contract gcp auditor jobs pay per year?

As of Aug 3, 2026, the average yearly pay for contract gcp auditor in the United States is $92,797.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $112,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Contract Gcp Auditor, you need a solid understanding of Good Clinical Practice (GCP) guidelines, clinical trial processes, and regulatory compliance, typically backed by relevant scientific or healthcare qualifications. Familiarity with auditing tools, electronic quality management systems (eQMS), and certifications such as ISO 19011 or formal GCP auditor training is highly valuable. Strong attention to detail, clear communication, and the ability to build rapport with stakeholders are crucial soft skills. These competencies ensure thorough, accurate audits that uphold regulatory standards and foster trust within clinical research teams.

What are the typical challenges faced by a contract GCP auditor, and how should candidates prepare for them?

Contract Gcp Auditors often face challenges such as navigating diverse clinical environments, adapting quickly to different sponsor or CRO protocols, and staying up to date with continually evolving regulatory requirements. Candidates should be prepared to manage varying audit scopes, maintain objectivity in complex situations, and balance multiple assignments with strict deadlines. Building a strong foundation in regulatory updates, proactive communication, and effective organizational skills will help auditors excel. Staying flexible and open to learning is key for success in this dynamic role.

What is a contract GCP auditor?

A Contract GCP Auditor is a freelance or temporary professional responsible for assessing clinical trials to ensure compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and company policies. They conduct audits of clinical sites, vendors, and internal processes to identify potential risks and ensure data integrity. Contract auditors typically work on a project basis for pharmaceutical companies, CROs, or regulatory agencies. Their role helps maintain ethical research standards and protects patient safety in clinical trials.

What cities are hiring for Contract Gcp Auditor jobs? Cities with the most Contract Gcp Auditor job openings:
What are the most commonly searched types of Gcp Auditor jobs? The most popular types of Gcp Auditor jobs are:
What states have the most Contract Gcp Auditor jobs? States with the most job openings for Contract Gcp Auditor jobs include:
What job categories do people searching Contract Gcp Auditor jobs look for? The top searched job categories for Contract Gcp Auditor jobs are:
Contract Gcp Auditor jobs near you
Infographic showing various Contract Gcp Auditor job openings in the United States as of July 2026, with employment types broken down into 72% Full Time, 11% Part Time, and 17% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $92,797 per year, or $44.6 per hour.

Clinical Quality Auditor

Astrix Inc

South San Francisco, CA • On-site

$60 - $75/hr

Full-time, Contractor

Re-posted 18 days ago

Job description

Our client is a patient-driven cardiovascular biotechnology company dedicated to advancing heart disease treatment by developing therapies that address the root causes of disease rather than managing symptoms alone.
Title: GCP Auditor
Location: Hybrid (3 days onsite, South San Francisco, CA)
Pay rate: $60-75hr+ Depends on experience
Schedule: Full-time, M-F 8am-5pm
Contract-to-hire
We are seeking a GxP Auditor to join a quality team in a contract-to-hire capacity. This role is ideal for a seasoned auditor with strong GMP experience who is looking to contribute to a growing organization while supporting and helping scale a global audit program.
Role Overview
The GxP Auditor will be responsible for executing and supporting audits across internal operations, vendors, and investigator sites, ensuring compliance with global regulatory standards. This individual will also play a key role in strengthening audit program infrastructure, supporting audit reporting, and managing CAPA lifecycle activities.
Key Responsibilities
  • Plan and conduct GxP audits (primarily GMP), including vendor and clinical/investigator site audits
  • Perform audit report reviews and ensure alignment with regulatory and quality standards
  • Support the audit lifecycle, including CAPA review, approval, and closure
  • Contribute to the development and improvement of audit program infrastructure
  • Collaborate cross-functionally with Quality and Operations teams
  • Participate in scheduled audits across multiple regions (domestic and some international travel)
  • Support upcoming GCP audits and ongoing audit planning activities
  • Travel: 20-50%

Qualifications
  • MUST be a Certified Auditor (required)
  • 5-10+ years of experience in Quality, Compliance, or GxP auditing/inspections
  • Strong working knowledge of FDA, EMA, ICH, and GMDP regulations
  • Hands-on experience conducting GMP audits (vendor and/or clinical site audits preferred)
  • Experience reviewing audit reports and managing CAPAs
  • Bachelor's or advanced degree in Life Sciences, Pharmacy, Chemistry, or related field
  • Experience in biotech/pharma environments
Preferred
  • Experience with MHRA and Health Canada regulations
  • Familiarity with Veeva and/or Smartsheets
  • Strong communication, collaboration, and stakeholder management skills

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