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Pharmacovigilance Co-ordinator

Qube recruitment
Posted 23 days ago, valid for 10 days
Location

Dartford, Kent DA4 9EA

Salary

£25,000 - £40,000 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Salary: Not specified
  • Experience Required: Minimum 3 years in Regulatory Affairs & Pharmacovigilance
  • Location: Dartford, UK
  • Responsibilities include developing and approving artwork components, liaising with project managers, coordinating with external pharmacovigilance contractors, and maintaining risk minimisation material
  • Qualifications include a degree in science or equivalent experience, proficiency in MS Office suite, and ability to work as a team player

Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator.

Job Description:

  • Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups.
  • Liaise with project managers for implementation of updated product information.
  • Co-ordinate with external pharmacovigilance contractors for submission of safety variations and PSUSA variations
  • Co-ordinate with pharmacovigilance contractors for updating and approval of risk minimisation material.
  • Responsible for maintaining and distribution of Risk minimisation material through external contractors.
  • Experience in uploading the product information to databases like EMC.
  • Review and provide sales data for PSUR reporting.
  • Conduct regular meetings with external pharmacovigilance contactors for the ongoing pharmacovigilance activities.
  • Responsible for ensuring all the relevant contracts are in place for pharmacovigilance activities carried out via external parties in UK & EU.
  • Responsible for completing detailed monthly PV Summaries.

Qualifications and Experience:

  • Educated to degree level in science or equivalent experience.
  • Minimum 3 years of experience in the Regulatory Affairs & Pharmacovigilance
  • Proficiency in the use of MS Office suite (Excel, PowerPoint)
  • Ability to take initiative and work with different departments as a team player within the organisation.

Monday to Friday: Full Time

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.