Regulatory Affairs Jobs in London

nCino offers exciting career opportunities for individuals who want to join the worldwide leader in cloud banking.Curious Minds. Bold Ideas. Extraordinary Impact.Were transforming financial services through bold innovation and relentless execution. You bring the ideas and drive. Well build whats nex...

Job DescriptionLead abest in classoncology medical affairs teamand work in collaboration withyourCross-functionalcounterparts to provide expert strategic input leading onValue and Implementation Medical Affairsobjectivesinthe Oncology therapeutic area.Youwillhold the overall responsibility for the d...

Job Description SummaryThe Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry Manufacturing and Controls. Successful candidates will be offered a training position consisting of two rotational assignments...

Job Description Summary#LI-HybridLocation: London (The Westworks) United KingdomWe are seeking a highly organised and collaborative Global RA Operations Resource Planner to join our Regulatory Affairs Operations team.In this role you will play a critical part in ensuring the effective planning and a...

We create a place where people can grow be their best be safe and feel welcome valued and included. We offer a competitive salary an annual bonus based on company performance healthcare and wellbeing programmes pension plan membership and shares and savings programme.We embrace modern work practises...

DescriptionJoin our Control Management team as a Vice President within Securities this dynamic role you will be at the forefront of managing the risk and control framework for primarily our in-business CDO ( Chief Data Office) and providing Business Control Management support for our Product Develo...

DescriptionThis is a full-time opportunity on a permanent basis. The role will be based in 10 South Colonnade Canary Wharf London E14 4PU.Government departments and agencies are working towards implementing a minimum 60% attendance in office sites.We are currently implementing a flexible hybrid way...

Job Description Summary#LI-Hybrid (12 days per month on-site if living within 50 miles of our London office)#LI-Remote (Homeworker if living further than 50 miles of our London office)Office Location: London (The Westworks) United KingdomWe are looking for a Global Labelling Manager Content to suppo...

Job Description Summary#LI-Hybrid (12 days per month on-site if living within 50 miles of our London office)#LI-Remote (Homeworker if living further than 50 miles of our London office)Office Location: London (The Westworks) United KingdomWe are looking for a Global Labelling Associate Director Conte...

Job Description Summary#LI-Hybrid (12 days per month on-site if living within 50 miles of our London office)#LI-Remote (Homeworker if living further than 50 miles of our London office)Office Location: London (The Westworks) United KingdomWe are looking for a Global Labelling Director Content to lead...

Ensure the development of appropriate business-focused high-quality timely regional regulatory strategy and its execution for assigned asset(s) consistent with relevant enterprise goals and respective product profile. This goal has to be achieved as a component of an overall global regulatory approa...

Job Description SummaryThe SSO Study Start-Up Manager is accountable for study planning SSU activities and activation deliverables of assigned projects in compliance with Novartis processes GCP/ICH and regulatory requirements in a standalone country OPC (operating country) or satellite country. Lead...

Job DescriptionClinical Research AssociateLocation: MidlandsTravel: Approximately 6575% (about 23 days per week domestic and international)About our company Our company is committed to advancing high-quality clinical research that upholds ICH/GCP standards and local regulatory requirements. We colla...

Medical Lead Respiratory Location: GSK Headquarters UK - Hybrid (23 days on-site per week)At GSK we are driven by a purpose: to unite science technology and talent to get ahead of disease together. As part of our Specialty Medicines team within the Chief Patient Officer Business Unit we are focused...

Job Title: Regulatory Affairs AssistantLocation:Pancras Square UKIntroduction to the RoleWerelooking for aRegulatory Affairs Assistantto join our Medical and Scientific Affairs this roleyoullprovideadministrative operational and compliance support to the Head of Regulatory and the wider Regulatory...

DescriptionJoin a Foreign Exchange Sales team at the forefront of FX innovation execution excellence and client satisfaction. As an Associate in FX Services Sales you will have the opportunity to shape the future of our FX platform drive FX Sales growth support own and manage FX account planning acr...

Clinical Medical ManagerShape the future of clinical development and bring life-changing therapies to patients faster through scientific excellence and strategic partnerships.Your new roleAs a Clinical Medical Manager youll be at the forefront of clinical trial excellence serving as the scientific...

The Senior Medical Director Oncology Clinical Development - GU will report to the Executive Medical Director Clinical Development Lead (CDL) Oncology Clinical Sr. Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSKs clinical portfolio...

About 3E:We are a mission-driven company dedicated to creating a safer and more sustainable world!3E provides award-winning regulatory expertise and cutting-edge technology that seamlessly integrates data and intelligence regarding chemicals regulations products and supply chains for over 5000 custo...

Title:Clinical Supply Chain Project ManagerCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience...