Job Title: Pharmacovigilance Co-ordinator
Employment Type: Permanent Position
Salary: £35,000 per annum
Location: Based in Kent. Hybrid (3 days on site)
Fantastic opportunity to work for a growing pharmaceutical company specialising in medicinal, non-medicinal, medical devices, and OTC products. The business is increasingly growing and is now looking for a PV Coordinator to join the team.
Key Responsibilities:
- 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.
Requirements:
· 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.
If this role is of interest please apply direct or send your CV to julie.ball@cpl.com