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| Job Title. | Location | Salary | Actions |
Clinical Trials AdvisorClinical 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, |
Limerick | Not Disclosed | |
Regulatory Affairs ConsultantRegulatory 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, |
Tipperary | Not Disclosed | |
Head of Regulatory AffairsHead of Regulatory Affairs Our client a new medical device company in Dublin currently seeks a Head of Regulatory Affairs. Successful candidate will be reLocation: Dublin, |
Dublin | Not Disclosed | |
Pharmacovigilance SpecialistPharmacovigilance 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, |
Tipperary | Not Disclosed | |
Regulatory Affairs ExecutiveRegulatory Affairs Executive Our client, based in Munster, is seeking a Regulatory Affairs Exec to join their consultancy. Work will be broad and will offer an excellent learning curve, even for experienced candidates. Responsibilities Ownership/ regulatory responsibility for a portfolio of products for nominated client and be responsible 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 strat...Location: Tipperary, |
Tipperary | Not Disclosed |
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Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: info@regulatoryaffairs.ie
Copyright © 2010 Life Science Recruitment Ltd | Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328 |
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Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: info@regulatoryaffairs.ie
Copyright © 2010 Life Science Recruitment Ltd | Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328 |
Web Design / SEO by WebScience | Valid XHTML - CSS





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