Every adverse event report that reaches CSL — from a treating physician, a license partner, a regulatory authority — starts its life in one place: intake. This role owns the quality of that starting point. Youll
We are recruiting Talent Management Executives to help ensure we have the best contractors working on our marketing campaigns. Working with household name clients your role will be to search for suitable contractors on our system and match
The role of the Enterprise Manager, EMEA Trade Compliance is responsible for the execution and maintenance of CSL’s world-class import-export compliance program in the EMEA Region. Its focus is to ensure all CSL legal entities operating
Senior Technical Designer – Medidata RAVE certified Join our growing team and discover your extraordinary potential by working as a Senior Technical Designer within our division, working with some of our most important sponsors. The position
JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are
About This Role: As a Senior Pharmacovigilance (PV) Scientist, you will play a pivotal role within the Safety team, serving as a product lead for Pharmacovigilance activities. You will be responsible for overseeing and leading safety
JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are
Role: Regulatory Associate – CTA Contract: 12-month rolling Office- Maidenhead (hybrid) – 3 days on site SRG are partnered with a global biopharmaceutical company with focus and capabilities to address some of the world’s greatest health
We are recruiting Talent Management Executives to help ensure we have the best contractors working on our marketing campaigns. Working with household name clients your role will be to search for suitable contractors on our system and match
Build and run the operating engine of CSLs PPP ( Public-Private Partnerships ) Centre of Excellence — the governance, methodologies, data, systems and internal network that let CSL evaluate, decide on, and execute government partnership opportunities at
Account Specialist Location: Maidenhead, England, United Kingdom (On-site at Abbott Maidenhead; occasional travel to Witney, Abingdon, or Central London may be required) Hours: Full-Time, 40 Hours per week (Monday - Friday) Flexibility: 8 hours per day
Communications Executive - London Overview of the Team The PR & Communications Team is responsible for communicating Londons growth narrative and positioning London & Partners as the authoritative voice on growth. Through its convening power and
Company Descriptionð Location: Maidenheadð¡ Hybrid Working: Minimum 3 days per week in the officeWere more than coffee.Were a global business worth over 5 billion, home to brands including Kenco, LOR, Tassimo, Douwe Egberts and Jacobs, serving millions
The role of the Enterprise Manager, EMEA Trade Compliance is responsible for the execution and maintenance of CSL’s world-class import-export compliance program in the EMEA Region. Its focus is to ensure all CSL legal entities operating
Join Maersk’s Groundbreaking Cyber Team: Redefining Incident Management & Response Imagine a career where youre not just responding to security incidents—you’re revolutionising how it’s done. At Maersk, one of the world’s largest and most respected logistics and
As Compliance Administrator at AVK, you provide essential administrative support to the Compliance team, ensuring that documentation, records and administrative processes are managed accurately, efficiently and in line with AVK’s compliance standards and data protection obligations.
Job Summary We are now recruiting a Senior Regulatory Affairs Manager, Europe supporting the Europe region and reporting to the Regulatory Affairs Director, Europe for Neuroscience & Specialty. By joining AbbVie you will play a pivotal
Regulatory Consultant – Clinical Trial Strategy & Submissions Location: Maidenhead - 3 days a week on site – Tues, Wed, Thurs Contract: 12 months We are currently seeking an experienced Regulatory Consultant to join a Clinical
Overview In this Senior PV Scientist role, you will lead pharmacovigilance activities for assigned products and act as a product lead within Safety. You will oversee signal management, literature reviews, and aggregate safety reports to support regulatory
Company: Ultra Intelligence & Communications Cyber (UK) Business Powering Decision Join the team redefining defense technology. From engineering systems that save lives to leading programs that change the battlefield—find your place in the future of defense. Cyber