Senior Pharmacovigilance Scientist
Term: Permanent
Salary: £33,750 - £42,750
Location: London
Our client are seeking a permanent Senior Pharmacovigilance Scientist to join their small Pharmacovigilance team on a permanent basis. They are a large, complex and dynamic company who offer a range of duties within the department.
Main Duties:
* To process Serious Adverse Event Reports (SAEs) from Clinical Trials
* To identify SUSARs and fulfil regulatory reporting requirements for SUSAR reporting to the MHRA and Ethics Committees
* To meet timelines on SAE data exchange with business partners
* To provide PV support and to keep abreast of safety issues on specified trials
* To support SAE-AE reconciliation as required
* To write Annual Safety Reports as required
Requirements:
* Life Science Degree
* 3 years in pharmacovigilance, ideally in an oncology clinical trials setting.
* Demonstrable experience in writing large Safety Reports
Periodic safety update reports safety signal detection clinical pharmaceutical biotechnology medical devices CRO clinical trials clinical development pharmacology health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative Argus SAE reconciliation safety PV DS PVG PVO SUSARs SARs
We are dedicated to the clinical research industry, offering candidates a unique service including our free \"Pipeline Watch\" career advisory consultation. To find out more call us on 0118 9594990 or email apply@clinicalprofessionals.co.uk
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