Reference Number: JO-1803-404810
Snr PV Director
Rate: Negotiable
Job Type: Permanent
Location: Greater London

Senior Pharmacovigilance (PV) Director
West London
Full Time / Office Based
Competitive Salary and Package

Our client a global Pharmaceutical giant are looking for a highly skilled Pharmacovigilance professional to join their West London team on a permanent full time basis. This exciting opportunity will allow any senior professional a high volume working environment with fantastic Pharma exposure

Successful candidate:
– Will ideally have 7 years plus experience in Pharmacovigilance
– A Life Science or relevant degree
– Extensive Regulatory and Safety experience (aggregate reports, safety submission, regulatory queries, CAPA management, Case Processing etc.)
– Previous experience in leading Operational Audits and Inspections
– Comply with all Global safety regulations
– Strong leadership and management skills
– Previous line management within a Pharma environment (including of training, delegating, and recruitment)

If the above is of interest, please call 01189 522 799 or email ashleigh.chambers@onlymedics.com

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

Clinical Professionals is a pan European life sciences 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, Medical Information, Compliance, Case Reporting, MHRA, FDA, EMA, Case Processing, QA, AE, Adverse Event, Quality Assurance, ARGUS, ARISG, Pharmaceuticals, Generics, Speciality, CRO, Clinical Safety, Risk Management, CAPA, PSMF, PSUR, DSUR, PBRER, Case Processing, PSMF, Pharmacovigilance System Master File, GVP, GPVP, CAPA Management, Auditing, Audit, CRO, Pharmaceutical, Biotechnology, Generics, UK, United Kingdom, England, South, South East, Berkshire, Surrey, Hampshire, Bedfordshire, Buckinghamshire, Sussex, Kent, Middlesex, Cambridgeshire, Oxfordshire, London

Upload your CV/resume or any other relevant file. Max. file size: 128 MB.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here