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Gcp Compliance Jobs (NOW HIRING)

ImmunityBio, Inc.

Senior GCP Auditor

$82K - $101K/yr

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 information

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$31.5K

$98.9K

$207.5K

How much do gcp compliance jobs pay per year?

As of Jul 29, 2026, the average yearly pay for gcp compliance in the United States is $98,949.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $115,000.00 per year, depending on experience, location, and employer.

Will compliance be replaced by AI?

GCP Compliance professionals focus on ensuring cloud environments meet regulatory standards and security requirements. While AI tools can assist with automating compliance monitoring and data analysis, human oversight remains essential for interpreting regulations and making strategic decisions. AI is a complement, not a replacement, for compliance roles in cloud security and governance.

What is a GCP Compliance job?

A GCP Compliance job ensures that an organization's use of Google Cloud Platform (GCP) follows industry regulations, security standards, and internal policies. Professionals in this role assess risks, implement compliance controls, and conduct audits to maintain regulatory adherence. They work with security teams, legal departments, and cloud engineers to ensure best practices. The role is essential for businesses in regulated industries like healthcare, finance, and government.

What is the highest paying job in compliance?

The highest paying compliance roles often include Chief Compliance Officer (CCO) and Director of Compliance, which can offer salaries exceeding $150,000 annually, especially in finance, healthcare, and technology sectors. These positions typically require extensive experience, leadership skills, and certifications such as Certified Compliance & Ethics Professional (CCEP) or Certified Regulatory Compliance Manager (CRCM).

Is compliance a dead-end job?

GCP compliance roles involve ensuring cloud infrastructure meets regulatory standards, which are critical for data security and privacy. These positions often require ongoing learning of evolving regulations and certifications, making them a stable career path with opportunities for advancement in cybersecurity and cloud management.

What are the key skills and qualifications needed to thrive in the Gcp Compliance position, and why are they important?

To thrive in a GCP Compliance role, you need in-depth knowledge of Good Clinical Practice guidelines, regulatory requirements, and quality assurance standards, often supported by a degree in life sciences or a related field. Familiarity with regulatory databases, electronic data capture (EDC) systems, and certifications such as Certified Clinical Research Professional (CCRP) or relevant GCP training are highly valued. Excellent attention to detail, strong communication, and the ability to work collaboratively are key soft skills for this position. These competencies are essential to ensure ethical conduct of clinical trials, maintain regulatory compliance, and support successful research outcomes.

How much do GCP compliance managers make?

GCP compliance managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and certifications such as CISSP or CISA. They oversee cloud security and regulatory adherence, often working with tools like Google Cloud Security Command Center and compliance frameworks like GDPR or HIPAA.

What are the common day-to-day responsibilities of someone working in GCP Compliance?

Professionals in GCP Compliance are typically responsible for monitoring clinical trial processes to ensure adherence to Good Clinical Practice guidelines, reviewing documentation for regulatory accuracy, and conducting internal audits or inspections. They frequently collaborate with clinical research teams, sponsors, and regulatory agencies to resolve compliance issues and provide training on GCP protocols. Daily tasks often include reviewing informed consent processes, overseeing data integrity, preparing compliance reports, and participating in risk assessments. This dynamic role requires meticulous attention to detail and regular communication across multiple teams to ensure the ethical and regulatory standards of clinical research are consistently met.

What cities are hiring for Gcp Compliance jobs? Cities with the most Gcp Compliance job openings:
What are the most commonly searched types of Gcp Compliance jobs? The most popular types of Gcp Compliance jobs are:
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Gcp Compliance jobs near you
Infographic showing various Gcp Compliance job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $98,949 per year, or $47.6 per hour.

Director - Quality GCP

Monte Rosa Therapeutics, Inc

Boston, MA • On-site

$185K - $235K/yr

Full-time

Posted 6 days ago

Job description

Overview
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!
Responsibilities
  • 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.

Qualifications
  • 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.

Apply