Scientific Officer - Pharmacovigilance

Ref. no.: 1777905

Tags: Quality Assurance Regulatory Affairs Compliance Pharmacovigilance

Location(s): Dublin City Centre Dublin North Dublin South

Salary range (€): Negotiable

Additional benefits: VHI,Educational assistance,Relocation package,Parking,Flexi Start,Canteen,Pension

Minimum experience required: 3 - 4 Years

Employment type: Permanent Full-time

Minimum qualification: See Description

Contact person: Ciaran McArdle

Contact e-mail: dublin@brunel.ie

Job description:  

Scientific Officer - Pharmacovigilance

Wonderful opportunity to work with market leaders within the pharmaceutical sector with a proven track record of developing their people. Excellent benefits and package on offer for the ideal candidate.

The role of the Scientific Officer - Pharmacovigilance is to assist in processing work through the Market Reporting to: Market Surveillance Assessor

Key Responsibilities:

· Coding, classification and evaluation of adverse event/reaction data

· Maintaining records of in-house and archived adverse reaction data

· Electronic reporting of adverse reactions to EudraVigilance/WHO/companies

· Preparing & compiling pharmacovigilance data for review, including as required:

· IMB database searches

· Requests for company searches

· EudraVigilance/WHO database searches

· Preparing activity reports for the Market Surveillance Unit

· Contributing to the monitoring of and preparation of IMB responses to non-urgent information (NUI)/rapid alert (RA) and other requests for information

· Contributing to the preparation of PV related publications

· Participating in the performance development programme (PDP) of the organisation and contributing to the setting of goals and objectives

· Taking measures to identify and resolve issues impacting on the performance of the Market Surveillance Section

· Performing such other duties as the Board may reasonably require

· Qualifications & Experience

The ideal candidate will have:

· Primary degree in a relevant life science discipline

· Postgraduate experience in the area of Pharmacovigilance/clinical trials/compliance monitoring

· Excellent knowledge of medicines legislation and guidelines

· Experience in the area of monitoring the safety of medicines (essential)

· Excellent communication, presentation, report writing and interpersonal skills

· Excellent organisational and computer skills

· Proven ability to work as part of a multi-disciplinary team

To apply for this position in strict confidence, please contact Ciaran McArdle in Brunel Recruitment on

+353 1 432 1510 or email your full CV to: cmcardle@brunel.ie

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