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Gcp Compliance Jobs (NOW HIRING)

Montefiore

Physician Assistant (JR229251)

Bronx, NY

$106K - $143K/yr

To maintain protocol and GCP compliance. * Responsible for providing proper explanation of study participation--including potential treatment options, alternatives to treatments, expected and ...

BioPhase Solutions

Medical Director

San Diego, CA · On-site

$350K - $385K/yr

Design early-phase trials and ensure high-quality study conduct and GCP compliance. * Author/review study documents and interpret emerging clinical data to guide decisions. * Lead/participate in ...

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How much do gcp compliance jobs pay per year?

As of Aug 23, 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.

Clinical Quality Assurance, Specialist II

Arrowhead Pharmaceuticals

San Diego, CA • On-site

$80K - $95K/yr

Full-time

Posted 9 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

The Clinical Quality Assurance Specialist will participate in the activities in support of the GCP and the Quality Assurance departments at Arrowhead to ensure compliance with GCP standards. This includes support in investigator audit programs, risk management plans, regulatory inspections, generating metrics for continuous improvement, and quality events while collaborating cross-functionally to uphold clinical trial quality and regulatory compliance.

Key responsibilities include assisting in GCP Quality Event management (non-conformances, deviations, CAPAs), contributing to risk-based audit planning, support in audits and inspections, SOP review and collaborating closely with the Clinical Operations team to ensure GCP compliance and data integrity.

Responsibilities

  • Develop and maintain clinical quality study risk plans and maintain updates in Quality Management System.
  • Collect site metrics for selection of investigator site audits while analyzing and reporting trends in audit findings.
  • Support and lead internal audits
  • Support QMS (Veeva) Audit entry, dashboard
  • SOP review
  • Facilitate ongoing quality improvement through communication of audit results, CAPAs and other quality events.
  • Issuance, tracking and completion of deviations, SCARs (supplier corrective action requests) and CAPAs.
  • Provide support for clinical study programs with GCP compliance, as needed.
  • Support health authority inspections.
  • Communicate any serious or critical compliance risks noted from these activities to senior management (manage report of Serious Breaches).
  • Keep up to date with all related quality legislation and compliance issues..
  • Support and contribute to risk management analysis efforts associated with GxP functions (primarily GCP).
  • Assist and/or support risk identification efforts at the asset / IP, therapeutic area, clinical study, clinical site, and vendor level.
  • Identify KPIs involved with risk monitoring from internal and external sources.
  • Communicate risk management mitigations and activities to the Manager Clinical Quality Assurance, Quality Assurance, and Clinical Operations and Development Teams.

Requirements

  • Bachelor's degree in science discipline is required.
  • 3 years of relevant experience in a regulated environment with preference to quality assurance, auditing and/or GCP experience.
  • 2 years of relevant experience in GCP function providing Quality and Compliance oversight.
  • Strong knowledge of GCP and Food & Drug Administration (FDA), European regulations and ICH guidelines.
  • Competent knowledge of and ability to use Veeva, Microsoft Word, PowerPoint and Excel
  • Requires occasional travel to other Arrowhead locations (San Diego, CA; Verona, WI; Pasadena, CA)

Preferred

  • Prior experience with use of an electronic document management system in a regulated environment is preferred (Veeva)
  • Knowledge of using Artificial Intelligence (AI) and/or building AI models (i.e., training dataset creation, validation, and reassessment) is beneficial.
California pay range
$80,000—$95,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

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