CLINICAL SAFETY MANAGER PHARMACOVIGILANCE jobs in United Kingdom

Clinical Safety Manager to join our UK team and to be based at our growing UK offices in London and Stirling. This position... and grow your career even further, then this is the opportunity for you. Responsibilities Manage Clinical Safety...

safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor Train new Clinical Safety Coordinators... for motivated individuals to join our Clinical Safety team in London. Working as part of a high performing group alongside Medical...

that ensures what we do, we do well. Responsibilities As the Senior Manager – Pharmacovigilance, you will be responsible...-cycle of assigned stand-alone safety and medical information projects, and the main pharmacovigilance point...

As a UK National Contact for Pharmacovigilance you will act as local Qualified Person for customers requiring the... IQVIA Lifecycle Safety Regulatory Intelligence Database (RID). · Availability on a 24/7 basis to receive calls from the...

, we rise to the challenge to make a difference and here’s how the Manager, Safety Surveillance & Risk Management role will make... within pharmacovigilance as a drug safety physician is preferential. Excellent time management skills and must be able to work to tight...

with a difference, ICON Strategic Solutions is the place for you. Responsibilities The role of the Manager Clinical Safety... and other functions within the company, as well as vendors for safety operational tasks. In addition, the Manager Clinical Safety...

that development safety update reports, pharmacovigilance reports and protocol amendments are submitted to MHRA, thereby maintaining... was established in 2008 to manage the sponsor responsibilities for Clinical Trials of Investigational Medicinal Products (CTIMPs...

. Closing date: 19 May 2024. Business unit: Research Management & Innovation. Department: KHP Clinical Trials Office.... Job description The QM is responsible for the KHP-CTO Quality Team which consists of: Senior Clinical Research Associates and teams...

development, including knowledge of applicable clinical trial safety regulations and postmarketing safety regulations. Includes...Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so...

sent by the Clinical Project Manager with the nationally approved texts of the product characteristics. Submits it to the... committees after discussion with the Clinical Project Manager. Informs him/her when the study can start. Manages the contract...

development, including knowledge of applicable clinical trial safety regulations and postmarketing safety regulations. Includes...Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so...