only medics  recruitment ltd

Pharmacovigilance Scientist

Croxley Business Park, Watford
40,000 - 60,000
17 Dec 2018
14 Feb 2019

Pharmacovigilance Scientist
Full time
Office based
Salary + bonus + company benefits

Exclusive to Clinical Professionals my client, a mid-sized pharmaceutical company are currently seeking an experienced Pharmacovigilance professional specialising within Safety Evaluation and Risk Management.
Successful candidate will have the following experiences:
A Life Science or relevant degree
Extensive former experience within a Pharmaceutical, Biotech or CRO
4+ years Pharmacovigilance experience
Authoring and writing of safety reports/aggregate reports including PSURs, DSURs, PBRERs
Safety Evaluation
Signal Detection
Risk management plans develop and implement
Project management desirable
Cross functional working and taking lead when required
Audit and Inspection support
Excellent verbal and written, influencing, presenting and communication skills

Please note in order for your application to be successful you must hold a valid right to work document for the UK as no sponsorship is offered.
If the above is of interest, please call +44 (0) 1189 522 799 or email

Specialist in contract, interim and permanent Pharmacovigilance staffing (Medical and Scientific) within the UK for Only Medics and Clinical Professionals, Europes Largest Life Science Recruiter.

Clinical Professionals is a pan European life science staffing business dedicated to the pharmaceutical, biotech, medical device, CRO and drug discovery industries. We provide clinical development, medical technology and commercial professionals to life sciences organisations on a permanent, retained, hosted contract, FSP and freelance basis across the UK and Europe. The Group is made up of Clinical Professionals, Only Medics and Regulatory Professionals. An award-winning organisation in the Global Recruitment Awards, APSCo and a full 3 star accredited organisation via the Times Top 100 Best Companies to work for. Clinical Professionals is part of the CPL Resources Group.

Key words:
Pharmacovigilance, PV, Drug Safety, Strategic Labelling, Labelling, Medical Information, Compliance, Safety Surveillance, Case Reporting, Epidemiology, MHRA, FDA, EMA, Case Processing, Patient Safety, Safety Lead, Eudravigilance, EVWEB, Gateway, QA, AE, Adverse Event, Quality Assurance, ARGUS, ARISG, Pharmaceuticals, Generics, Speciality, CRO, Post Market Surveillance, PMS, Clinical Safety, Risk Management, CAPA, PSMF, PSUR, DSUR, PBRER, Post Marketing, Case Processing, PSMF, Pharmacovigilance System Master File, GVP, Good Clinical Practice, GPVP, CAPA Management, Auditing, Audit, CRO, Pharmaceutical, Biotechnology, Generics, EU, Europe, UK, United Kingdom, Ireland, Nordic, England, London Glasgow, Liverpool, Edinburgh, Birmingham, Bristol, Cardiff, Leeds, Manchester, Belfast, Newcastle, York, Yorkshire, Sheffield, Nottingham, Cambridge, Oxford, Coventry, London, City of London, Brighton, Southampton, Portsmouth, Kingston upon Hull, Aberdeen, Plymouth, Norwich, Manchester, Swansea, Leicester, Dundee, Bath, Derry, Stoke-on-Trent, Sunderland, Derby, Peterborough, Wolverhampton, Bradford, Chester, Reading, Newport, Milton Keynes, Exeter, Preston, Bournemouth, Durham, Chichester, Stirling, Salford, Inverness, Canterbury, Middlesbrough Berkshire, Surrey, Hampshire, Bedfordshire, Buckinghamshire, Sussex, Kent, Middlesex, Cambridgeshire, Hertfordshire, Oxfordshire, London, Willing to relocate, Home based, Remote

Similar jobs

Similar jobs