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Job Title. Location Salary Actions

Pharmacovigilance Associate

Experienced Pharmacovigilance Associate required in Dublin West

Location: Dublin, Dublin Greater, Dublin West,
Pharmacovigilance Associate 		Dublin € Negotiable

Clinical Trials Advisor

Clinical Trials Advisor Responsibilities: -Analysis of clinical trial protocols and other client source material -Build up a thorough knowledge of the trial -Preparation of study materials for development teams; -Determine what elements are important to the target audience and the depth of coverage required in the product -Script product content to meet client requirements and in-house quality Standards -Identify leverage from previous trials -Resolve clinical queries from the development teams -Storyboard with Graphic Designers as part of graphic development -Review and sig...

Location: Limerick,
Clinical Trials Advisor 		Limerick Not Disclosed

Regulatory Affairs Consultant

Regulatory Affairs Consultant Responsibilities: Ownership/ regulatory responsibility for a portfolio of products for nominated clients and responsibility for close liaison with the Management / other key personnel of the relevant business unit in the definition of product strategies in line with timeframes for approval. Proposes and implements effective strategies to minimise the timing of and optimise the commercial viability of product licenses. Responsibility for the preparation of Package Leaflet User-Test or Bridging Reports. Builds and maintains strong relationshi...

Location: Tipperary,
Regulatory Affairs Consultant 		Tipperary Not Disclosed

Pharmacovigilance Specialist

Pharmacovigilance Specialist Our client, a Consultancy based in Munster, is seeking a PV Specialist to join their organisation on a permanent basis. Responsibilities: To complete the duties of a Qualified Person and/or Deputy (QPPV) Writing of Periodic Safety Update Reports and searching for ADRs Assessing adverse reactions for potential signals Producing summary safety tables for Client review Preparation and training for Regulatory Inspections MedDRA coding Understand...

Location: Tipperary,
Pharmacovigilance Specialist 		Tipperary Not Disclosed
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