Pharmacovigilance Manager, PVE Manager, Pharmacovigilance & Epidemiology Manager
A long-term 12-month contract has become available for an experienced PVE Manager. You will be working at one of the world’s top Pharmaceutical companies, based at their Cambridgeshire site, responsible for the operational support of clinical studies as well as case processing to external parties.
You will be responsible for following internal processes to ensure sufficient compliance is met with industry standards, as well as ensuring appropriate safety exchange measurements are taken between the company and CROs for clinical trials.
Safety language in contracts.
Vendor oversight of safety information reporting for global Patient Assistance and Support Programs.
Authoring Pharmacovigilance agreements (PVA) with license partners and CROs. Pharmacovigilance training.
PV compliance and quality measures.
Sitting within the world’s leading players in the pharmaceutical industry, this company continue to develop and offer a magnitude of innovative medicines onto market. Ranging from HIV, oncology, inflammation, respiratory and cardiovascular conditions. Now with a global stamp this company is worldwide recognised as a leading research based organisation.
This position would be suitable for an experienced consultant with a strong understanding of drug safety requirements.
At least 5 years Pharmaceutical industry experience.
Project Management experience.
Strong knowledge of global safety requirements.
Contract Length – 12-months.
Location – UK - Cambridge
Rate Circa: 60 per hour
They are looking to shortlist candidates in the next coming days and so do not hesitate to apply.
Please contact Keeley Munday on 02030196022 or email your CV to email@example.com