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Pharmacovigilance Risk Management Specialist



Business Type: Pharmaceutical Company, Healthcare Company, Pharmaceutical Services
Job Type: Clinical - Drug Safety
Job Level: Experienced (non manager)
Position: Contract
Location: Cambridgeshire
Reference: NS7392013
Closing Date: 18/06/19
Job Details:

Pharmacovigilance Risk management Specialist
Cambridge- office based
Company- Biopharmaceutical
Contract: 18 months
Paying lucrative hourly rate (7.5 hours a day)


INTRO:

A fantastic opportunity has arisen for a PV Medical Writer to a well established global biopharmaceutical company in Cambridge. You will be in a supportive Risk Management team and responsible for signal detection work and authoring RMPs and Aggregate reports.

Responsibilities include:

* Authoring of PSURs/PBRERs and DSURs
* Authoring risk management plans
* Signal detection and authorship of signal work-up documents
* Reviewing global literature
* Performing risk/benefit evaluation



REQUIREMENTS:

* Bachelors in a Life Science Degree
* Prior experience working within Pharmacovigilance in either a CRO or pharmaceutical industry
* Experience in writing PSURS/DSURs
* Experience writing Risk management Plans
* Clinical or post-marketing experience
* Working knowledge of ICH GCP and regulatory guidance
* Excellent organisational skills
* Motivated personality and must be able to work with strict timelines

This is a great chance for an ambitious individual to really develop their career in a supportive environment.

To Apply
If you would like to discuss this vacancy further, please call i-Pharm Recruitment Consultant Niki Sansoy on +44 (0)20 3189 0470 or email nsansoy@i-pharmconsulting.com.
ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

Key Words: Pharmacovigilance/ Drug Safety / CRO / Pharma / UK



Posted: 21/05/2019 | NPJ Ref: 235966
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