Reference Number: JO-1804-407422
Drug Safety Specialist
Rate: Negotiable
Job Type: Contract
Location: Greater London

Safety Data Specialist
West London
Full Time / Office based
Contract: 12 months (initially)
Rate: Competitive freelance rate
**Multiple openings**

Our client, a global Pharmaceutical giant have a unique opportunity for a Safety Data Specialist to join their rapidly growing organisation by offering multiple openings for a 12 month contract. The role focuses on coordinating the receipt of case reports and completing follow up events

Successful candidate will ideally have experiences in:
– Life Science or relevant degree
– 1+ years experience within Pharmacovigilance
– Retrieving cases in IRT
– Data Entry – ARISg desired
– Adverse Events
– Computer literate with expert knowledge of the Global Safety Databases ARISg desired
– Excellent organisational skills and self-dependant
– Excellent written and oral communication skills

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

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