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Job Ref.: 1683

Job Title: Pharmacovigilance Executive (with Risk Plan Management Responsibility) - Pharmaceuticals - Dublin West - October 2018 - Urgent

Sector: Pharmacovigilance

Location: Ireland, Dublin West

Job Type: Permanent full-time

Job description:

Pharmacovigilance Executive (with Risk Plan Management Responsibility) - Pharmaceuticals - Dublin West - October 2018 - Urgent

Our client, a major pharma company based in Dublin currently have a vacancy for an experienced Pharmacovigilance Executive to work within their PV department.

This is a permanent full-time position. The position will report into the Head of PV.

Responsibilities

  • Main task will be to assume Risk Management Plans full operational responsibility.

  • Fulfil the role of Local Safety Responsible (LSR) back-up.

  • Assume as a back-up operational Pharmacovigilance responsibility for ensuring that the collection, reporting and handling of safety information associated with company products is performed according to company global and local regulatory requirements.

  • Fulfil as a back-up the role of Market Research and Patient Support Program (MAP) Pharmacovigilance Approver.

  • Ensure prompt and accurate responses to safety queries from internal and external sources.

  • Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development.

  • Take personal responsibility for maintaining high ethical standards and operating in compliance with local and global company policies, the Company Group Code of Conduct, Quality Management System and the IPHA Code of Practice for the Pharmaceutical Industry.

  • Fulfil all tasks delegated by the LSR in a timely and compliant fashion.

Skills Profile

  • Clinical background, i.e. life sciences, nursing, health care or pharmaceutical experience is desirable

  • Regulatory background, preferably with over two years in RMP management

  • Ability to write clear, concise, unambiguous medical text

  • Ability to acquire knowledge in different disease and therapeutic areas

  • Understanding of drug development process & drug safety regulatory obligations

  • Proven good communication skills with an international perspective

  • Excellent attention to details

  • Knowledge of medical terminology

  • Excellent time management

  • Able to interact well within a team setting

  • Able to interact cross-functionally

  • Agile

An excellent salary plus bonus and benefits package will be offered to the successful candidate

For further information, please contact Paul Flanagan at Dublin (01) 805 5522 or e mail your c/v in the strictest confidence paul@pharmasolutions.ie

 

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