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Gcp Compliance Jobs (NOW HIRING)

NCSL International

Director of GCP Quality

Princeton, NJ · On-site

$123.09 - $184.63/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 ...

TRI Challenge Convention

PRINCIPAL, QA

Bethesda, MD · On-site

Verifies GCP compliance to applicable Standard Operating Procedures (SOPs) and regulations Conducts audits of clinical sites and vendors/suppliers Provides full support to the Quality Management ...

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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.

What cities are hiring for Gcp Compliance jobs?

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

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What states have the most 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, Clinical Quality Assurance (GCP)

Eikon Therapeutics

Jersey City, NJ • On-site

$204K - $246K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Job description

Position  

We are seeking an experienced and dynamic Director, Auditor, Clinical Quality Assurance to lead our GCP auditing efforts. The successful candidate will play a pivotal role in ensuring that our clinical trials adhere to Good Clinical Practice (GCP) guidelines and maintain the  highest standards of quality. This includes internal audits, site audits, and vendor audits.   

This role requires a minimum of 3 days per week onsite (or more, as business needs require) in either our Jersey City (NJ), or Millbrae (CA) offices.

About You  

You are an expert-level auditor with the discipline and consistent follow-through to see complex audit programs through to completion. You are an excellent communicator who builds trust and collaborates effectively with stakeholders. You thrive as part of a dynamic team, and you're motivated by the opportunity to drive projects and results while mentoring and developing others.  

What You'll Do  

  • Lead and manage the Clinical Quality Assurance (CQA) audit program, ensuring compliance with GCP, applicable regulations, and company SOPs.  
  • Provide leadership, mentorship, and functional guidance to CQA staff and/or contract auditors, and contribute to departmental strategy, budget, and resource planning.  
  • Lead quality management system (QMS) assessment for service providers and collaborate closely with Clinical Development Vendor Oversight team to ensure service provider qualification process is robust and timely.  
  • Develop and execute risk-based audit plans, conduct audits of clinical trial activities, and provide timely and accurate audit reports.  
  • Provide expert guidance to cross-functional teams on GCP compliance, protocol adherence, and regulatory requirements.  
  • Collaborate closely with the Clinical Operations team to identify and address quality related issues, deviations, and non-compliance events.  
  • Review and approve essential study documents, including protocols, informed consent forms, and clinical study reports.  
  • Contribute to the development of procedural documents (e.g., SOPs and WIs).  
  • Develop and implement GCP training programs for internal staff and external partners/vendors involved in clinical trials.
  • Own and lead inspection-readiness strategy across the clinical development portfolio, including planning and facilitating mock inspections.  
  • Represent the company in regulatory inspections and audits and lead the preparation and response efforts.  
  • Stay abreast of industry trends, regulations, and best practices related to clinical quality assurance and GCP.  

Qualifications  

  • 12+ years of progressive experience in clinical quality assurance or a related field in the pharmaceutical or biotechnology industry with a Bachelor's degree, or 10+ years of   
    equivalent experience with an advanced/post-graduate degree. Additional certifications (e.g., RAC, CQA) highly desirable. 
  • Extensive knowledge of GCP guidelines, ICH E6(R2), and other relevant regulatory requirements.  
  • Strong leadership, analytical, and problem-solving skills, with meticulous attention to detail and accuracy.  
  • Exceptional communication and interpersonal skills, with a proven ability to lead and collaborate in a cross-functional team environment.  
  • Demonstrated experience in conducting clinical trial audits and inspections.  
  • Previous experience in pharmacovigilance auditing is a plus.  
  • Expertise in Veeva systems is a plus  
  • Ability to travel up to 50% (domestic and international).

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:

  • 401k plan with company matching
  • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
  • Mental health and wellness benefits
  • Weeklong summer and winter holiday shutdowns
  • Generous paid time off and holiday policies
  • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
  • Enhanced parental leave benefit
  • Daily subsidized lunch program when on-site

The expected salary range for this role is $204,000 to $246,750 depending on skills, competency, and the market demand for your expertise.

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