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Senior Specialist, Country Study Start Up
The Sr. Specialist Country Study Start Up proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country or countries. The Sr. Specialist Country SSU is responsible and accountable for on-time budget and quali...
Senior Specialist, Government Affairs Uki
Primary Function of Position:The Government Affairs Senior Specialist will work with the Director Government Affairs UK/I supporting the development and execution of a high impact Government Affairs strategy. This includes: development of messaging and materials for a variety of external audiences i...
Recruitment Data Policies Eu Labeling, Advertising...
Make your mark for patientsWe are looking for a Labelling Advertising and Promotion Scientist (EU) who is collaborative detailminded and adaptable to join our Global Labelling Promotion and Advertising team based in any of our Brussels (Belgium) Monheim (Germany) or Slough (UK) offices.About the rol...
Regulatory Compliance Analyst Remote
About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco our investors include Benchmark General Catalyst Peter Thiel Adam DAngelo Larry Summers and Jack Dorsey. Position: Insurance Regulatory Compliance Specialist Type: Contract...
Insurance Compliance Specialist Expert
About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco our investors include Benchmark General Catalyst Peter Thiel Adam DAngelo Larry Summers and Jack Dorsey. Position: Insurance Regulatory Compliance Specialist Type: Contract...
Senior Regulatory Affairs Specialist
JOB DESCRIPTION:Senior Specialist Regulatory AffairsLocation: WitneyAbbott is about the power of health. For more than 130 years Abbott has been helping people reach their potential because better health allows people and communities to achieve more. With a diverse global network serving customers i...
Global Manager, Performance Validation Personal Ca...
About UsElementis is a global specialty chemical company with 1300 employees operating 17 manufacturing sites across the globe. At Elementis we bring a distinctive combination of expertise innovation and teamwork to every formulation challenge. We create high-value specialty additives that enhance t...
Senior Nonclinical Writer (remote Uk)
Are you looking to join a company where your contributions truly matter and where youll be part of a supportive innovative teamMMS is aaward-winning data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization recognized for our exceptio...
Senior Nonclinical Writer (remote Uk)
Are you looking to join a company where your contributions truly matter and where youll be part of a supportive innovative teamMMS is aaward-winning data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization recognized for our exceptio...
Specialistsnr Specialist Study Start Up And Regula...
The Senior Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and external stakeholde...
Eu Regulatory Affairs Manager (biosimilars)
Career CategoryRegulatoryJob DescriptionIf you feel like youre part of something bigger its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togethe...
Director Cmc Regulatory Processes And Systems
Title:Director CMC Regulatory Processes and SystemsCompany: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 exp...
Director, Regulatory Affairs
Your work will change lives. Including your own.The Impact Youll MakeRecursion is at the forefront of reimagining drug discovery and development through broadening the funnel of potential targets using technology and standardization to build connected data and superlinearly scaling our efforts to ac...
Regulatory Affairs Manager, Oncology Therapeutic G...
Regulatory Affairs Manager Oncology Therapeutic Group Global Regulatory AffairsClosing Date: 30th October 2026 (COB)Business IntroductionAt GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering an...
Regulatory Affairs Manager, Oncology Therapeutic G...
Regulatory Affairs Manager Oncology Therapeutic Group Global Regulatory AffairsClosing Date: 7th September 2026 (COB)Business IntroductionAt GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering a...
External Supplier Quality Specialist
Reporting to the Manager Supplier Quality Management (EMEA) this role is responsible for the quality oversight of suppliers across the EMEA region. The successful candidate will manage supplier quality activities throughout the supplier lifecycle including qualification quality risk management chang...
Sr. Specialist, Supplier Quality Management (emea)
Reporting to the Manager Supplier Quality Management (EMEA) this role is responsible for the quality oversight of suppliers across the EMEA region. The successful candidate will manage supplier quality activities throughout the supplier lifecycle including qualification quality risk management chang...
External Supplier Quality Specialist
Reporting to the Manager Supplier Quality Management (EMEA) this role is responsible for the quality oversight of suppliers across the EMEA region. The successful candidate will manage supplier quality activities throughout the supplier lifecycle including qualification quality risk management chang...
Global Cpq Developer
Are you a current Elekta employee Please click here to apply through our internal career site Find Jobs - Elekta.We dont just build technology. We build hope for everyone dealing with Cancer.Elekta is shaping the standard of care together with healthcare providers by developing precision radiation m...
Recruitment Data Policies Global Legal Immunology ...
Make your mark for patientsGlobal Legal Immunology Lead UK & IrelandWe are looking for aGlobal Legal Immunology Lead UK & Ireland who is strategic collaborative and pragmatic to join us in our Legal teambased in our Slough office in the United Kingdom.About the roleAs Global Legal Immunology Lead UK...