UK Home-Based / W London / M4 PhV QA Director / Associate Director SME on Patient Support
This role is graded Director or Associate Director and comes with a Stock Plan, Performance Bonus, higher than usual pension, and car allowance. My client offers a merit-based environment for applicants who are considering a career change in 2018 and want to make their mark in a global R&D and marketed products QA PhV function. You will be the QA SME for Patient Support Programs specifically, as well as for internal sites, inspections readiness and new systems rollouts (for PhV QA/Drug Safety QA). Faraway audits are completed by a vendor and you will be joining a central QA team of PhV of 8 professionals so this is not a solo operation. Lastly before I explain more about the role, I am looking for a real expert, so someone who is easily at Associate Director or Director grade! The company are investing a very healthy 23% of T/O for their R&D programmes, across 4 therapeutic streams which include mAbs, and this role can be based in Bucks South, Berkshire, Middlx or in West London / SW London / Surrey borders. There is some flexibility for the UK if you do not live close to the site, in terms of spending some time working from home (audit travel max 30%). Please consider the following for this role:- Would you like to work in a corporate drug development and research based pharmaceutical company, and be visible and supported for your Quality advisory? Are you looking for a role where you are part of the senior team to review and assess Risk, co-develop the audit plan and implement in a mix internal / vendor audit model? Are you someone who wants to be involved with the therapy groups, often by data review, to support the business, and be able to, with integrity, sign off on new products which are highly innovative, often mAb/fAbs, and where there is high unmet medical need? Are you interested in supporting Patient Support programmes, early access initiatives and other patient centric platforms (e-monitoring / devices)? Would you like to collaborate with sites and business systems, to provide QA support for Drug Safety systems and new processes? Do you want to ‘audits’ but not spend more than 30% of your time on the road auditing? Are you looking to work in a team which has a merit based advanced systems and where your ideas matter? We would welcome hearing from anyone who would like to be considered for this role, and has existing QA Pharmacovigilance experience, or ICH GCP and CSV with some exposure to PhV audits or inspections or systems. This role is not a CSV role but we are seeking someone who is happy working with both clinical / observational data and systems. The company offers a relocation policy for the UK, as well as a strong package, including Stock, RSUs, Bonus, Car and progressive salary banding. The leader of the group has a strong reputation for developing people and is not new to people management. We like her vision for quality, so why not call me in confidence and I will explain who my role is for and her vision, approach and requirements. ___________________________________________________________________________________________ Please contact me, Matt Greig, at Advanced Regulatory for more information and a confidential applicant. I work extended hours most days and can be reach on +447918679405 - alternatively please send your CV with a covering note to email@example.com ___________________________________________________________________________________________ About Advanced Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas - we have offices both in the UK and in Switzerland. We are a recruitment business dedicated to the pharmaceutical industry. Keywords / Key words: ICH GCP, QA PhV, Quality Jobs, Jobs in QA, Audit Manager, Audit Senior Manager, Audit Director, PhV QA, Jobs in PhV QA, Jobs in Quality Assurance, Jobs in GCP Compliance. To Apply : Please send a full CV in confidence to firstname.lastname@example.org.