Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

Google Chrome
Internet Explorer
Mozilla Firefox

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job






Salary Expectations:



Current Location:

Notice Period:

Write here your cover note:

If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to

Pharmacovigilance Officer

Reference:AHSR-282413 Location: Roscommon
Qualification:DegreeExperience:2-3 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Pharmacovigilance

Pharmacovigilance Officer

Our Client, One of the leading health care business in Britain and Ireland based in Roscommon is currently sourcing for Pharmacovigilance Officer. The PV Officer is responsible for carrying out pharmacovigilance activities in accordance with Good Pharmacovigilance Practices and company Quality Management Systems for the company and clients where applicable.

The Role

• Screen worldwide (local) scientific literature on a weekly basis and evaluate relevant information for inputting on to an internal database.
• Evaluate adverse event reports received directly from regulatory authorities and input relevant reports onto an internal database
• Process safety data arising from all source as per SOPs
• Report safety data using EudraVigilance
• Input into extended EudraVigilance Medicinal Product Dictionary
• Prepare and participate in regular signal detection meetings
• Prepare and ensure submission of PSURs and Risk Management Plans in a timely manner.
• Update Pharmacovigilance System Master File as required.
• Ensure identified safety variations are planned, tracked and sent as per set timelines in accordance with the legislation.
• Prepare weekly reports for the Regulatory Manager and QPPV.
• Ensure compliance with Volume 9A of The Rules Governing Medicinal Products in the EU and GVP modules, Reg 1235/2010, Reg 520/2012 and directive 2010/84/EU as applicable, and also the company procedures
• Identify and implement practices to improve the Pharmacovigilance system including review of SOPs as required.
• Attend external meetings/training courses to maintain/improve overall knowledge of Pharmacovigilance procedures, guidelines and directives.

The person

• Third Level qualification in a scientific discipline
• The role demands a well-organised approach, underpinned by the ability to communicate effectively with people at all levels, both verbally and in writing.
• Reliability, IT literacy and the ability to plan and complete projects to set timelines is essential.

If you would like further Information you can contact the recruiter directly:

Jannet Diana | Tel: +353 (0) 1 507 9255

Planner Pharmaceutical Cork Quality Auditor Westmeath Healthcare MES Consultant Medical Device Biopharmaceutical Medical Affairs QA Manager Clinical Research Quality Specialist EHS Engineer Engineering Supply Chain Coordinator Biomedical Engineer Contract Senior Scientist Supply Chain Sales Development Executive Validation Manager Formulation Scientist Kildare Sales Consultant Bioprocess Engineer BD Manager Regulatory Affairs Manager QA RA Engineer Regulatory Affairs Specialist Engineering Supply Chain Administrator Chemist Nurse Associate Technical Writer Principal Scientist Validation Engineer Pharmacist PhD Biochemist Quality Control Manager Research Scientist Dublin North Supply Chain Specialist Galway Automation Software Controls Manager Project Engineer Process Development Engineer Dublin Food Scientist QA Specialist Republic of Ireland Life Science Project Lead Regulatory Affairs Validation Scientist EHS Specialist Project Manager Academic Scientific Sales Quality Control Supervisor Dublin South Quality Manager Formulation Chemist Medical Advisor Academic Supply Chain Scientific Sales Specialist Process Engineer Biotechnician Engineering Manager Contract Sales Executive Equipment Engineer QC Analyst QA Supervisor Biotechnology Quality Assurance Officer Validation Coordinator Manufacturing and Technology Manager R and D Manager Regulatory Affairs Automation Engineer Scientist Qualified Person Connected Health Research and Development Scientist Dublin West Validation Specialist Senior Research and Development Engineer Manufacturing Engineer Biotechnologist Quality Systems Lead Limerick Life Science QA Analyst Manufacturing Coordinator Account Manager Accountant QA Executive Chemistry Nationwide Microbiology Sligo Biostatistician Medical Director Quality Assurance Quality Systems Specialist