Harlow, London, United Kingdom Hybrid / WFH Options
Teva
ways to continue making a difference, and new people to make a difference with. We would like to invite applications for the role of Pharmacovigilance Associate for UK&IE to oversee the smooth running of the UK/IE Case Management team activities and related processes, ensuring the handling of … accordance with local/EU legal requirements. Location : Harlow. We have a hybrid approach to home working! A day in the life of a Pharmacovigilance Associate... Case Management: Triaging of spontaneous and solicited ICSRs and SAEs received by Teva for authorised and marketed anddevelopment products in UK/IE Entering … Completion of the quarterly Global outcome pregnancy trackers Completion of the Daily line listing Reconciliation of ICSRs and SAEs exchanged between UK/IE Pharmacovigilance and relevant Teva UK/IEinterfaces Managing any UK/IE case related queries and escalating any complaints/medial queries/health authorityrequests to more »
have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications more »
their complex business challenges. As part of the team, you will focus on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You'll Do Lead multiple project engagement teams empowering the team to plan and manage all aspects of more »
Hatfield, Hertfordshire, United Kingdom Hybrid / WFH Options
Confidential
leads, and partakes in Eisai Business initiated projects and other ad hoc activities where required. What are we looking for? Demonstrated experience in a Pharmacovigilance role. Prior experience with SDEAs and building relationships with PV partners. In depth knowledge of Pharmacovigilance regulatory reporting requirements in European countries Graduate level education more »
top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance).As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers in the research and development (R&D) space – managing teams more »
