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Senior Associate Global Safety

* 10 month contract, Top Biopharmaceutical Company, Senior Associate Global Safety – Cambridge *

My client a top Biopharmaceutical Company has a need for a Senior Safety Associate to join their Safety team.

Within this role you will be working within the UK and Ireland Affiliate Safety Department, and reporting to the Global Safety Senior Manager, this role will be responsible for ensuring adherence to the company's regulatory commitment for pharmacovigilance.
You will perform a wide variety of safety activities within the local affiliate, based on sound knowledge of local legislative requirements and company procedures. The role involves collaboration with other affiliate functions and also with Global Safety colleagues to meet business needs.


KEY RESPONSIBILITIES

Ensures complete and timely internal and external reporting of national/international adverse events for products used in clinical trials and marketed products
Ensures compliance with local and international safety regulations and procedures
Records, screens and categorises reports of adverse drug reactions in clinical studies
Coordinates tracking and evaluation of adverse drug reaction reports
Compiles and submits reports on cases of suspected adverse drug reactions to authorities
Updates standard safety information documents and procedures
Participates in international safety forums/meetings
Reports adverse events to internal sources and external regulatory authorities
Collects and provides follow-through resulting in timely and accurate to reporting and archiving
Collects, analyses and communicates information regarding safety profiles for developing/marketed products Screens local literature for expediting safety reports
Categorises incidents and safety concerns
Provides information response to internal and external customers regarding developing and marketed products 

To be considered for this role you must have a Life Science / Pharmacy degree.
You will possess experience of a Drug Safety / Pharmacovigilance role within the industry including case processing, pre and post market activities. Argus experience is a plus.

Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.

To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on 0203 465 0045.


Summary

Job Type:
Contract
Industry
Pharmaceuticals
Location
Cambridge
Specialism
Life Sciences
Pay
£20 - 24 p/h
Ref:
3232396
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Talk to a Consultant

Talk to Roberta Atkins, the specialist consultant managing this position, located in London City

107 Cheapside, London, EC2V 6DN

Telephone: 0203 465 0045
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