Advarra

Pharmaceutical Quality GCP Auditors Freelance/Independent (Consulting)

Advarra  •  London, GB (Onsite)  •  1 month ago
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Job Description

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Location

This role is open to candidates based in United Kingdom.

Company Information

At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.

Company Culture

Our people--both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.

Advarra is seeking Good Clinical Practice (GCP) Auditors to join our consultant network for United Kingdom -based projects. Auditors support compliance reviews across GCP clinical sites and vendors.

Job Duties & Responsibilities

  • Conduct Good Clinical Practice (GCP) audits (planning, agenda, physical or remote audit, and report writing)
  • Evaluate investigator sites, CROs, and vendor compliance or qualification.
  • Prepare comprehensive audit reports detailing findings and root-causes.
  • Provide written audit reports in English.
  • If required will provide corrective actions support and present findings to QA leadership and stakeholders
  • Work collaboratively with clients to ensure quality standards.

Basic Qualifications

  • Minimum 10+ years of Clinical Quality Assurance and/or Good Clinical Practice (GCP) experience.
  • Minimum 5+ years of Good Clinical Practices auditing experience.
  • Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities.
  • Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans.
  • B2 level in English communication, verbal and written
  • Bachelor's degree

Preferred Qualifications

  • Strong interpersonal and client interaction skills.
  • Excellent analytical, problem-solving, communication, and report-writing skills.
  • Ability to work collaboratively across departments and interact with internal and external stakeholders.
Advarra

About Advarra

Advarra advances the way clinical research is conducted: bringing life sciences companies, CROs, research sites, investigators, and academia together at the intersection of safety, technology, and collaboration. With trusted IRB and IBC review solutions, innovative technologies, experienced consultants, and deep-seated connections across the industry, Advarra provides integrated solutions that safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance. Advarra is advancing clinical trials to make them safer, smarter, and faster. For more information, visit advarra.com.

Industry
Biotech & Life Sciences
Company Size
1,001-5,000 employees
Headquarters
Columbia, Maryland
Year Founded
1983
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