CK Group is recruiting for a permanent Pharmacovigilance Scientist to join a global pharmaceutical company, whose main site is located in Bracknell.
Main Responsibilities:
- Deliver 100% compliance with respect to adverse event/reaction reporting timelines. Ensure ICSR processing is compliant with company procedures, including internal and regulatory timelines.
- Ensure follow-up information is requested in accordance with company procedures and timelines utilising the Product Quick Guide and query reports where appropriate..
- Develop strong cross-functional relationships and assist business partners in navigating and complying with PV relevant procedures.
- Support PV audits and inspections
- Support PV agreement activities
- Maintain a strong working knowledge of relevant PV legislation, regulations and company procedures.
As a Pharmacovigilance Scientist you will require the following:
- Minimum of 2 years experience within Pharmacovigilance
- Pharmacovigilance knowledge on a process and compliance level.
- Life Science degree or equivalent
- Previous experience of pharmacovigilance and working within regulatory requirements within the pharmaceutical industry (essential)
Apply:It is essential that applicants hold entitlement to work in the UK. Please quote job reference 54411 in all correspondence.
