Pharmaceutical Quality GCP, MHRA Mock Inspector

Job not on LinkedIn

🔥 14 hours ago

🇬🇧 United Kingdom – Remote

⏱ Part Time

🟠 Senior

🔴 Lead

👻 Ghost score 10%

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Advarra

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1983

💼 Consulting

📦 Logistics

📣 Marketing

Consulting • Logistics • Marketing

Advarra is a provider of integrated technology and services for clinical research, combining institutional review and compliance services with software platforms to support the full clinical trial lifecycle. The company offers ethics review services (IRB, IBC, DMC, endpoint adjudication), site enablement and research staffing, and a suite of cloud products — including eRegulatory, eConsent, eSource/EDC, CTMS and study design tools — plus an AI-powered operational intelligence engine (Braid) to streamline trial start-up, enrollment, and operations. Advarra serves sponsors, CROs, research sites, and institutions with a focus on patient protection, regulatory compliance, and accelerating trial outcomes.

📋 Description

• Conduct Good Clinical Practice (GCP) mock inspections, including planning, agenda, physical investigation, coaching, and report writing • Evaluate Sponsors, CROs, and investigator sites • Prepare comprehensive inspection reports detailing findings • Provide written inspection reports in English • Work collaboratively with clients to ensure quality standards

🎯 Requirements

• Candidates must be based in the United Kingdom • Registration in the Advarra consultant network is required to be considered • Minimum 10+ years of Quality Assurance and/or Good Clinical Practice (GCP) experience • Minimum 5+ years of Good Clinical Practice (GCP) inspection experience • Demonstrated work history with MHRA (Medicines and Healthcare products Regulatory Agency) • Demonstrated experience in leading, developing and conducting investigation activities • B2 level in English communication, verbal and written • Bachelor's degree • 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

🏖️ Benefits

• Inclusive and collaborative work environment • Respect for diverse perspectives • Opportunity to make a meaningful impact on clinical research • Consultant network opportunities for UK-based projects

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