Pharmaceutical Quality GCP EMA Mock Inspector – Consulting

🔥 14 hours ago

🇬🇧 United Kingdom – Remote

⏱ Part Time

🟠 Senior

🔴 Lead

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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 • Join Advarra's consultant network for EU-based projects

🎯 Requirements

• 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 at any European Health Authority • 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 • Registration is required to be considered if not already part of the consultant network

🏖️ Benefits

• Inclusive and collaborative work environment • Respect for diverse perspectives • Opportunity to make a meaningful impact advancing clinical research

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