and monitoring activities for the SSA team. CAPA Support: Support Corrective Action and Preventative Action (CAPA) plans and their effectiveness checks. Skills and Qualifications: Pharmacovigilance Knowledge: Pharmacovigilance and drug development, including clinical trial and post-marketing safety regulations. Knowledge of case processing, expedited reporting rules, and safety database concepts. Aggregate more »
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 »
medical qualification or PhD in a topic relevant to the position is beneficial. Experience working in a clinical drug development environment. Previous experience in pharmacovigilance, including advanced knowledge of PV regulation and cross-functional working. Strong knowledge of international pharmacovigilance requirements, specifically in the UK, Europe and US Salary and more »
inform decision-making and drive innovation. Compliance and Regulatory Oversight: Ensure all medical affairs activities comply with relevant regulations, guidelines, and ethical standards, including pharmacovigilance, medical information, and promotional practices, and provide strategic guidance on regulatory submissions and compliance initiatives. Requirements: Education: Advanced degree in life sciences (MD, PharmD, PhD 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 »
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 »
