REGULATORY COMPENSATION EXPERT jobs in CAMBRIDGE, United Kingdom

and theories; Serves as consultant to RA in area of vendor expertise Expert knowledge of and interprets new regulatory... possible, together. Job Description Regulatory Affairs Vendor Governance is a function within the RA Business Operations group...

for knowledge for their product to these key stakeholders Deep and expert understanding of the regulatory environment leveraging... possible, together. Job Description Regulatory Affairs Associate Director Gilead Sciences, Inc. is a research-based...

activities of an international portfolio of subcontractors, diverse and high-tech product portfolio As a Quality expert... particularly clinical supply chain teams. Management. Direct consultants on complex projects Act as a subject matter expert...

activities for SO related processes. We are seeking a PS expert to manage and support the execution of strategy and ensure.... Expectations for the above activities includes understanding of global PV regulatory requirements related to the collection...

inspection and audit activities for SO related processes. We are seeking a PS expert to manage and support the execution... includes understanding of global PV regulatory requirements related to the collection, processing and submission of ICSRs...

possible, together. Job Description Description: Serves as a senior scientific and clinical expert for safety profile of products... and initiatives based on deep understanding of good pharmacovigilance practices (GVP) and other regulatory guidance Participates in...

possible, together. Job Description POSITION OVERVIEW: Develops or oversees and ensures that strategic scientific and regulatory... subject matter expert (SME) support to the PS TA on behalf of Benefit-Risk Science and Process team (BRSP) into signal...

into study-related activities and documentation, regulatory submissions, responses to regulatory agency inquiries... RESPONSIBILITIES: Serves on cross-functional Global Development Teams as the safety expert, go-to-person, for safety profile...

and quality manner. You will also provide input on behalf of MSS into study-related activities and documentation, regulatory... submissions, responses to regulatory agency inquiries, pharmacovigilance (PV) processes and projects, and PV or other audits...