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Job Details

Pharmacovigilance Associate

Company: ProClinical Ltd
Location: Slough
Reference: DS.RE.17529
Closing Date: 26 Jul 18
Type: Permanent
Salary (£): 30,000 - 40,000
Benefits:

Job Summary:

ProClinical is working with a global specialty pharmaceutical group that is seeking a Pharmacovigilance Associate to be based in Slough. This Associate role will assist the Local Pharmacovigilance Manager (LPM) in the provision of a comprehensive, accurate and timely local Pharmacovigilance (PV) management service for the UK and Ireland, within the framework of all applicable Standard Operating Procedures (SOPs). ...

Requirements:

ProClinical is working with a global specialty pharmaceutical group that is seeking a Pharmacovigilance Associate to be based in Slough. This Associate role will assist the Local Pharmacovigilance Manager (LPM) in the provision of a comprehensive, accurate and timely local Pharmacovigilance (PV) management service for the UK and Ireland, within the framework of all applicable Standard Operating Procedures (SOPs).

Job Responsibilties:

* Completing local pharmacovigilance (PV) activities in accordance with company Standard Operating Procedures (SOPs) and Working Instructions (WIs).
* Process Individual Case Safety Reports (ICSRs) and ensure timely completion of all case processing activities in line with local regulations and company requirements.
* Logging of adverse events into the Medical Information database as required and transferring reports to Global Patient Safety (GPS).
* Determine and perform appropriate case follow-up, generating follow-up letters.
* Working in collaboration with GPS on case processing activities.
* Filling ICSRs.
* Provide information and conduct Pharmacovigilance training to the company staff and third-party providers.
* Reconciliation of all adverse event reports from Third Party service providers, distributors and licence partners.
* Managing the local literature review process, conducting reviews (on-line and hardcopy non-indexed journals) to identify potential ICSRs and to identify safety information in accordance with company SOPs.
* Perform monthly legislation scanning.
* Maintain awareness of PV regulatory requirements and developments.
* Management of departmental email inbox.
* Organise off-site archiving of PV case files

Skills and Requirements:

* A Life Science graduate with at least 1 year’s work experience in pharmacovigilance or previous pharmacovigilance experience within the life science industry
* Comfortable working within a commercially-focused environment
* Possessing good telephone manner and oral and written communication skills
* A proficient user of standard MS Office software
* A working knowledge or awareness of Pharmacovigilance Legislation
* Self-motivated and organised

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Rebecca Eaton on +44 203 8001 292 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Apply for this job: Pharmacovigilance Associate

Contact Information:

Address:  ProClinical Ltd
Eldon House Eldon Street London
EC2M 7LS
England
Tel:  0800 988 4437
Fax:  +44 (0)207 834 9470
Website:  Visit Our Web Site

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