REGULATORY AND CLINICAL PROJECT jobs in EUROPE ENGLAND, United Kingdom #3

on our business. About the Role: As a Regulatory Affairs Manager, you will play a pivotal role in leading a team of Project... of Project Managers and Regulatory Affairs Specialists focused on the UK market. Managing all regulatory activities relating...

lives. Read more: The European Regulatory Procedural Strategist (ERPS) team leads and manages the procedural... and operational aspects of the European regulatory filings within the European Centralised Procedure, working in close collaboration...

of product development from clinical to lifecycle. Support may include organizing, managing and executing on regulatory CMC...CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in...

advice to project teams to ensure continued regulatory compliance and timely market release. Support external regulatory...CK Group are recruiting for a Regulatory Partner (Medical Devices) to join a company in the Pharmaceutical industry...

that regulatory requirements are met for Clinical Trial Applications that involve Medical Devices of any nature (e.g. physical devices... regulatory advice to project teams to ensure continued regulatory compliance and timely market release. Support external...

in clinical studies. You will provide operational and technical regulatory assistance through all stages of clinical... regulatory input during clinical development to ensure compliance of diagnostics used in therapeutic trials with global and local...

teams; ability to broadly represent the regulatory functions on project teams within BMS and across alliance. Experience... clinical trials in communicating between Diagnostic sponsor and Drug sponsor. Experience as a member of Global Regulatory sub...

About The Role Job Title: Head of Clinical Pharmacy Role Purpose: Are you a visionary leader passionate... about delivering exceptional pharmaceutical services? Join us as the Head of Clinical Pharmacy to ensure the highest standards...

IQVIA UK are seeking Senior Clinical Research Associates to strengthen our cFSP (sponsor dedicated) business unit..., initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good...

, Pharmacovigilance, Real World Evidence, Project Management, Regulatory, Clinical Data Science and Clinical Development Globally..., and other clinical, regulatory and safety documents as required. With limited supervision may participate in or lead departmental...

clinical trial personnel, Clinical Operations, Data Management, Clinical Development, Medical Affairs, Regulatory Affairs... right to work in this location. Responsibilities: Manage clinical logistics and participate in cross-functional project...

, data management, clinical development, medical affairs, regulatory affairs, technical operations, manufacturing, MSAT... Responsibilities: Support clinical logistics & participate on cross-functional project teams. Could be assigned to program management...

training events in partnership with Senior Project Leaders, Clinical Leads, and clients. Plan and manage equipment...Are you a dynamic leader with a passion for education and clinical trials? Vitalograph is seeking a dedicated Clinical...

through quality related activities; Provide project/program leadership in quality as a team member across clinical development...+ years of pharmaceutical industry experience in GCP quality assurance or regulatory affairs or clinical development...

templates, CRF completion guidelines, Clinical Monitoring Plans. Develop additional study tools specific to the project.... Job Description Primary Function of Position: The Clinical Research Associate (CRA) is a critical role principally performing remote on-site...

dedicated to facilitating high quality clinical trial supply. We work closely with departments such as Clinical Project... highest quality standard. You will become part of LEO Pharma Clinical Supply Management. We are a team of five professionals...

Job Overview Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines... regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions Evaluate audit findings...