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Job Details

PV Associate

Company: SciPro
Location: Cambridge
Reference: PVA 01
Closing Date: 12 Apr 17
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

I am recruiting for my Cambridgeshire based client for a PV Assocaite to join their team on an inital 6 month contract. Candidates must have case processing experience, using the ARISg database. This is an excellent opportunity for candidates seeking to broaden their safety knowledge in both a clinical trial and post-marketing setting and to be part of a progressive department.

Requirements:

Key attributes/Skills/Education

* The candidates will ideally be a life sciences graduates and have experience of working in Pharmacovigilance.
* Competent with medical terminology, excellent communication abilities and possess good IT skills.
* Previous use of a safety database (preferably ARISg or Argus web based) is required.
* A high standard of organisation, narrative writing and impeccable attention to detail is essential.

This is an excellent opportunity for candidates seeking to broaden their safety knowledge in both a clinical trial and post-marketing setting and to be part of a progressive department.



Working in a global Pharmacovigilance Department the candidates will gain exposure to many different aspects of Pharmacovigilance. Following induction to the company and training, the Pharmacovigilance Associates will be responsible for:

* Case processing including data entry, narrative writing, review and assessment of SAE/AE reports from all sources (incl. clinical trial and post marketing) onto our global safety database.
* MedDRA coding.
* Case submissions to regulatory authorities.
* SAE reconciliation.
* Literature review.
* Using and maintaining the global safety database.
* Contributing to the ongoing enhancement of Pharmacovigilance processes and writing Standard Operating Procedures.
* Safety data retrieval, supporting information requests production of data for aggregate reports.
* Supporting the Pharmacovigilance team with the production and quality control of safety reports in CSRs, DSUR/PSURs, and regulatory dossiers (MAA/NDA).

* The candidates will ideally be a life sciences graduates and have experience of working in Pharmacovigilance.
* Competent with medical terminology, excellent communication abilities and possess good IT skills.
* Previous use of a safety database (preferably ARISg or Argus web based) is required.
* A high standard of organisation, narrative writing and impeccable attention to detail is essential.

Apply for this job: PV Associate

Contact Information:

Address:  Head Office
4th Floor, 150 Leadenhall Street, London
EC3V 4TE
England
Tel:  +44(0)203 327 3072
Website:  Visit Our Web Site

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