GVP Pharmacovigilance Auditor - Homebased

NonStops Client is currently seeking an experienced clinical research GVP (Pharmacovigilance) auditor, potentially with additional GxPs auditing experience

You will be available and eligible to travel across UK / Europe as required, without travel restrictions and be available to travel circa 40-50% of the working time.

You will be an established lead clinical investigator site auditor with a high level experience and knowledge of European/EMEA regulatory requirements and industry guidelines governing global PV / GCP

You will preferably be living in the UK or Ireland, or possibly in mainland Europe - close to a main European connecting airport. Fluent spoken and written English to a high level is imperative and additional languages beneficial, although not essential.

The client is a leading full service GxP QA Specialist organisation, with true global reach, and a growing team of successful QA auditing professionals working across GxP auditing specialisms with multiple industry leading clients, vendors / CRO's.

As part of their continued UK/EU/EMEA audit team growth, they seek an experienced PV Auditor to work fully remote - home based.

You will undertake a range of rewarding and challenging solo Pharmacovigilance GVP audits for multiple Clients and Vendors, including; Investigator Sites / CRO's and Laboratories involved in Clinical Research.

Additionally, you may from time to time undertake additional GxP audits - Preference for GCP or GLP auditing experience. You should have experience in at least one other GxP.

Key things to be able to succeed in your new role.

• Solid knowledge of international regulatory requirements desired + Industry guidelines governing GCP (Good Clinical Practice), GVP, GLP - ICH, EMA, MHRA and local European regulations
• Ability to assimilate and analyse information rapidly
• Life Science Degree minimum. BSc / MSc. PharmD, PhD
• Current resident and working in Europe
• Home Based. With eligibility to travel as required without travel restrictions
• Registrations, accreditations or certifications - Preferred

• 3+ Years Solo/Lead GVP (Good Vigilance Practice) Pharmacovigilance Auditing experience required
• 7+ Years QA Quality Assurance and PV Auditing experience required - Clinical Investigator Sites, CROs, Labs and Vendors in UK / Ireland or Europe
• Solid working knowledge and understanding of all European Quality and PV regulations
• Post marketing PV/Pharmacovigilance audit experience desired

If this role is of interest to you then do not hesitate to get in contact today as my client is looking to select suitable CV's in the next week. Please send your CV in MS Word format (I am unable to accept PDF copies!) to me directly, Ruby Wallace, at r.wallace@nonstop-recruitment.com, or by calling me on 02079402105 for a discussion in confidence.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.