| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | Essex |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Senior Pharmacovigilance Auditor, Market Leading CRO A well-established and market leading CRO based in Essex are now searching for a Senior PV Auditor to join their well-experienced and close-knit team. Their pharmacovigilance team is growing due to increased demand, new clients, and product expansion. This is an exciting opportunity to work with an ever-expanding and diverse portfolio, ranging from support services relating to COVID-19 vaccines through to end-to-end support for gene therapies. As well as a brand-new stunning office in 2018, this company offers amazing training, internal personal development schemes and a great social environment where you can flourish. This is an opportunity that offers great job stability and longevity with a cutting edge CRO that are growing year-on-year. You will act as lead pharmacovigilance auditor in this role which will hold you responsible for the managing and conducting of pharmacovigilance audits for clients, people management and oversight, maintenance and management of the companys internal pharmacovigilance programme and collaborating with leads of other teams in pharmacovigilance. You will build and manage the auditing team at your new company, grow the auditing function within the business, utilising your expertise, knowledge and experience of best-practice methodologies and practices in industry, working closely with senior management to ensure a solid audit plan is in place for clients. To succeed in this role, you should have extensive experience within the drug safety and auditing space.Your responsibilities include:- People management: oversee and manage staff, regular 1-1 coaching with direct reports, coach and guide staff in all aspects of PV auditing, performance review, training, recruitment, succession planning- Operational: acting as lead PV auditor, managing and conducting audits for clients, managing and maintain a schedule of audits for clients, manage the internal PV programme- Processes and systems: develop processes and procedures to ensure best practices are adhered to, improve client service and efficiency, ensure staff follow company processes- Collaboration across PV, evaluating and improving quality management, building the audit businessYou can be home-based for this role, but will be required to travel if and when audits are taking place. You should be an effective communicator, have a proactive approach and confidently be able to present your ideas effectively.If youre interested in this role, click apply now to forward an up to date copy of your CV, or call us now. If this job isnt quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Required skills
Keyskills :
CRO seni audit Life Science pharmaceutical quality quality assurance officer auditing audit pharma drug safety pharmacovigilance pv biotech associate case processing pvqa