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Gcp Compliance Jobs (NOW HIRING)

Jade Biosciences

Director, Clinical Compliance

$210K - $235K/yr

Serve as a trusted GCP compliance advisor to all functions within study teams by promoting a culture of quality and helping teams integrate compliant practices into daily study execution and decision ...

NKW NantKwest 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 ...

ImmunityBio

Senior GCP Auditor

Culver City, CA · On-site

$88K - $108K/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 ...

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 ...

Legend Biotech USA

Director of GCP Quality

Princeton, NJ · On-site

$122.72 - $184.09/hr

Ensure that GCP compliance in alignment with Genmab's Quality Policy, procedures and regulatory requirements * Maintain a risk-based approach for conducting trial site audits, process audits and ...

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$98.9K

$207.5K

How much do gcp compliance jobs pay per year?

As of Aug 22, 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.

What is a GCP Compliance?

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 does a GCP Compliance do?

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 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.

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

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Gcp Compliance jobs near you
Infographic showing various Gcp Compliance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% 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

$185K - $235K/yr

Full-time

Re-posted 23 hours 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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