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 »
within the Clinical Science team. This hire will work closely with a multidisciplinary team including biostatisticians, regulatory affairs, clinical operations and data management, toxicologists, pharmacovigilance, medical affairs, market access, etc as necessary. This hire will be based in the UK, working remotely from there. As a medical expert, you will 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 »
Surrey, England, United Kingdom Hybrid / WFH Options
Planet Pharma
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 »
