CLINICAL SAFETY MANAGER PHARMACOVIGILANCE jobs in ENGLAND, 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...

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...

. Job Description We have a new opportunity within our Drug Safety function for a Manager, Drug Safety. This role provides clinical safety... and pharmacovigilance support to medicines across life-cycle. Reporting to the Head of Drug Safety, you will oversee the drug safety...

. Job Description Manager, Quality Management within Strategic Operations, Patient Safety The Patient Safety (PS) department is a global... function that is part of the Development organisation within Gilead. The main Pharmacovigilance activities of PS are centered...

, 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...

. 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...

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...