7 of 7 Permanent Pharmacovigilance Jobs in England

Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems, etc. Consulting experience, working with a major system integrator or software vendor. Regulatory Affairs, Regulatory Operations or Pharmacovigilance background. Knowledge of Pharmaceutical, Biotechnology, and/or Medical Device and Diagnostics regulatory processes, data and content. PMP certification. Execution experience with Agile methodology and/or ACP Certification. Life More ❯

acquiring new projects to support our customers to deliver on their complex business challenges. 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 delivery, from scope to quality More ❯

choice for 85% of the 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 and planning, organizing, and More ❯

choice for 85% of the 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 Consultant, you will manage workstreams on consulting projects for Veeva customers in R&D - planning, organizing, and tracking all aspects of delivery. You will analyze problems, build More ❯

best professional staffing firm, and 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 from all suitably qualified candidates More ❯

Leadership Teams, Business, Business Processes, Business Process Management (BPM), Change Management, Contract Management, Cross-Functional Teamwork, Decision Making, Employee Training Programs, EU Legislation, Leadership, Management Process, Negotiation, People Leadership, Pharmacovigilance, Program Implementation, Project Implementations, Project Management System, Regional Management, Regulatory Compliance, Regulatory Experience, Regulatory Intelligence, Regulatory Strategies, Regulatory Strategy Development + 5 more Preferred Skills: Job Posting End Date More ❯

provide scientific and commercial expertise, defining new service offerings that will create a competitive advantage. Reporting to the Head of the Late Phase business unit, your expertise will include: Pharmacovigilance and Safety Observational studies and Patient Registries Interventional studies HEOR Real world evidence Managed/Expanded access programs As Vice President, Subject Matter Expert, Late Phase you will be expected More ❯