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Advarra

Pharmaceutical Quality GCP, MHRA Mock Inspector

Advarra

. Conduct Good Clinical Practice (GCP) mock inspections, including planning, agenda, physical investigation, coaching, and report writing .

Posted 11/7/2026part-timeRemote • United KingdomSeniorLeadWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates extensive experience in Good Clinical Practice (GCP) inspections and Quality Assurance, with a strong ability to prepare detailed inspection reports and collaborate effectively with clients and stakeholders.

Highest-signal resume keywords
Good Clinical Practice (GCP) Inspection ExperienceQuality Assurance ExperienceMHRA Compliance KnowledgeB2 Level English CommunicationAdvarra Consultant Network Registration

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
GCP Mock InspectionsInspection Report WritingQuality Standards EvaluationAnalytical SkillsProblem-Solving Skills
Soft Skills
Interpersonal SkillsClient Interaction SkillsCollaborative Work
Certifications & Qualifications
Bachelor's DegreeAdvarra Consultant Network Registration
Industry Keywords
MHRAClinical TrialsInvestigator SitesCROsQuality Assurance

About the role

Key responsibilities & impact
  • 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

What you’ll need
  • 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

Comp & perks
  • 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