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Gcp Compliance Manager Jobs (NOW HIRING)

6149-DePuy Synthes Products Inc. Legal Entity

$102 - $177/hr

... Compliance Manager DePuy Synthes is recruiting for a Clinical and Pre-Clinical QA Compliance ... Additionally, this role will include GCP projects relative to supporting compliance activities ...

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Gcp Compliance Manager information

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$38.5K

$95.1K

$157K

How much do gcp compliance manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for gcp compliance manager in the United States is $95,103.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What does a GCP Compliance Manager do?

A GCP Compliance Manager is responsible for ensuring that an organization's operations and activities within Google Cloud Platform (GCP) comply with relevant regulations, standards, and internal policies. They develop and implement compliance frameworks, monitor cloud usage for risks, conduct audits, and coordinate with legal, IT, and security teams to address any issues. Their role helps organizations avoid regulatory penalties, maintain data security, and build trust with clients and stakeholders when using GCP services.

What are some typical challenges a GCP Compliance Manager faces when ensuring continuous adherence to regulatory standards?

A GCP Compliance Manager often encounters challenges such as keeping up with evolving regulatory requirements, coordinating compliance efforts across multiple teams, and managing documentation for audits. They must work closely with clinical operations, quality assurance, and regulatory affairs to ensure all trial activities meet Good Clinical Practice (GCP) standards. Proactively identifying compliance gaps and effectively communicating expectations are key to maintaining high-quality standards and avoiding costly delays or regulatory findings.

What are the key skills and qualifications needed to thrive as a GCP Compliance Manager, and why are they important?

To thrive as a GCP Compliance Manager, you need in-depth knowledge of Good Clinical Practice (GCP) guidelines, regulatory requirements, and experience in clinical trial oversight, usually supported by a life sciences degree and relevant compliance certifications. Familiarity with electronic trial master files (eTMF), audit management systems, and regulatory databases is essential. Attention to detail, strong communication, and problem-solving abilities help ensure effective collaboration and issue resolution. These skills and qualities are vital for maintaining regulatory compliance, protecting patient safety, and supporting successful clinical research outcomes.

What is the difference between Gcp Compliance Manager vs Cloud Security Engineer?

AspectGcp Compliance ManagerCloud Security Engineer
CertificationsGCP certifications, compliance frameworksSecurity certifications (CISSP, CISA, etc.)
Work EnvironmentCloud compliance teams, security compliance rolesSecurity architecture, threat mitigation in cloud environments
Industry UsageOrganizations managing GCP compliance requirementsOrganizations implementing cloud security measures

Gcp Compliance Managers focus on ensuring organizations meet GCP-specific compliance standards, while Cloud Security Engineers implement security measures to protect cloud infrastructure. Both roles require knowledge of cloud platforms, but their primary responsibilities differ: compliance versus security implementation.

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Gcp Compliance Manager jobs near you
Infographic showing various Gcp Compliance Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $95,103 per year, or $45.7 per hour.

Specialist II, Quality Compliance

Corcept Therapeutics

Redwood City, CA

$90K - $115K/yr

Full-time

Posted 13 days ago

Job description

The Quality Specialist II of Quality Compliance will be a core team member of the Quality Compliance department to perform day-to-day Quality operations as instructed and trained to support success of the clinical studies sponsored by Corcept.

The Specialist II, Quality Compliance supports the Clinical Quality Compliance function by assisting with GCP compliance activities, vendor oversight processes, audit program administration, quality system activities, inspection readiness efforts, and continuous improvement initiatives. This role partners closely with Clinical QA, Clinical Operations, Pharmacovigilance, Biometrics, and external vendors to help maintain compliance with applicable GCP regulations, industry standards, and internal procedures. The Specialist will support the planning, coordination, execution, and follow-up of audits and quality system activities and may participate in  audits under the guidance of experienced QA auditors.
This is a hybrid role typically requiring on-site presence at least 3 days per week.

Responsibilities:

  • Support vendor qualification, monitoring, and requalification activities, including documentation reviews and risk assessments
  • Coordinate vendor, and internal GCP audits in accordance with the annual audit plan
  • Support audit logistics, scheduling, documentation management, agenda preparation, and audit communications
  • Assist in preparing audit reports, tracking observations, and monitoring audit-related CAPAs through closure
  • Maintain audit records, audit schedules, and audit metrics within Veeva QMS and other quality systems
  • Participate in GCP audits as an audit team member and develop auditing skills through training, mentorship, and on-the-job experience
  • Assist with vendor performance monitoring and tracking of key vendor quality metrics
  • Support quality agreement development, revision, execution, and periodic review activities
  • Participate in inspection readiness initiatives and continuous improvement projects designed to strengthen GCP compliance across the organization
  • Assist in the development and maintenance of quality metrics, reports, and dashboards
  • Identify opportunities for process improvement and support implementation of quality and compliance initiatives
  • Maintain awareness of evolving GCP regulations, industry guidance, and best practices

Preferred Skills, Qualifications and Technical Proficiencies:

  • Excellent in basic Microsoft Office applications (Word, Excel, PowerPoint) is required
  • Basic understanding of GCP and best industry practices

Preferred Education and Experience:

  • A BA/BS degree in biological sciences, pharmacy, or a related field is required
  • 2-4 years' experience in clinical-stage pharmaceutical companies or a related field

Travel

  • Up to 25% following certification as auditor

The pay range that the Company reasonably expects to pay for this headquarters-based position is $90,000 - $115,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

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