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Gcp Compliance Manager Jobs (NOW HIRING)

ImmunityBio, Inc.

Senior GCP Auditor

$82K - $101K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ensures compliance with SOPs and ICH GCP E6 (R2) standards. * Manages the incident management program through monitoring of complaints, deviations and CAPAs. * Schedules, plans, coordinates, and ...

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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 Aug 14, 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 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.

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 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 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 cities are hiring for Gcp Compliance Manager jobs?

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

The most popular types of Gcp Compliance jobs are:

What states have the most Gcp Compliance Manager jobs?

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What job categories do people searching Gcp Compliance Manager jobs look for?

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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 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $95,103 per year, or $45.7 per hour.

Director Quality GCP

Monte Rosa Therapeutics, Inc

Boston, MA • On-site

$185K - $235K/yr

Full-time

Posted 22 days ago

Job description

Monte Rosa Therapeutics is seeking a Director Quality GCP to provide strategic oversight of phase-appropriate  Quality GCP and GCLP activities, including GCP quality oversight of ongoing quality activities supporting active pre-clinical and clinical programs through participation on in-house and external cross-functional teams.  This role requires an 75% on-site presence. You will work closely with industry leaders in Boston and Basel . Join a diverse, collaborative, and dynamic team that values innovation, teamwork, and a people-centric culture!


  • Primary GCP Quality contact for identified vendors and investigator sites supporting clinical programs as well as other GCP quality events (e.g., potential serious breach assessments, CAPAs)
  • Author key GCP quality SOPs and key reviewer for other quality (GxP) procedures.
  • Develop a risk-based GCP compliance program.
  • Support teams in the initiation, review, and closure of quality events and associated CAPA, Change Action, and Effectiveness plans.
  • Develop and provide GCP and other GxP training (as applicable).
  • Ensure appropriate qualification of vendors and ensure compliant vendor management and regular assessment/audits. May conduct GCP audits (vendors and sites).
  • Ensure audit observations are communicated, tracked and remediated.
  • Provide QA GCP review and feedback on regulatory submissions.
  • Lead and participate in inspection readiness activities for regulatory inspections – both internally and at clinical sites.
  • Interface with internal departments and external vendors on a variety of technical/quality subjects.

  • BS Degree in Chemistry, Pharmacy, Biology or a related life science, or a combination of a BS Degree with relevant Quality and Technical experience.
  • Minimum of 16 years of experience within the pharmaceutical or biopharmaceutical industry, with development experience and exposure to commercial operations.
  • Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus.
  • Able to provide solution-minded approach and flexibility to emerging challenges.
  • Able to appropriately balance priorities plus multi-task against competing priorities.
  • Proven experience with the desire, and ability to work in a fast-paced, matrixed, start-up environment.
  • Hands-on leader, able to provide solution-minded approach and flexibility to emerging challenges
  • Understanding of drug development and program management preferred.

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