Overview

Reference Number: JO-1801-367709
PV Associate
Rate: Negotiable
Job Type: Permanent
Location: London

Pharmacovigilance Associate
West London
Permanent
Full Time / Office based
Salary offering circa. 25,000 per annum

My client, a Japanese pharma, are seeking a PV associate to join their team on a permanent basis. This is an excellent opportunity for anyone with PV experience to be able to grow and progress their career with a reputable, global company with a strong pipeline.

Responsibilities
ICSR reporting
Case processing – clinical and post market
Use of ARGUS database
Ensure all PV activities are conducted in accordance with global SOP’s
Liaise with EU and Asian offices

Skills/Experience/Abilities/Qualifications
Between 1-2 years experience within Pharmacovigilance
ICSR reporting/submission
Case processing – clinical and post market
Excellent organisational skills
Excellent written and oral communication skills
Previous use of ARGUS database

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

Alternatively, you can apply to this job and others using an online CV profile. Click the link below to create an account and submit your online CV.