Regulatory Documents Jobs in Aberdeen Sct
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Job Profile Role
A Bit About Us
Role Details Regulatory Affairs Manager EMENA PharmaceuticalsRole:Full-timePermanentLocation:Stockley Park LondonSalary:Competitive bonus benefitsThe Role Wereseekingaproactive and meticulousRegulatory Affairs Manager to oversee ourRegulatorylifecycle activities(managing submissions regulatory cha...
Sr Mgr. Regulatory Affairs
Regeneron Pharmaceuticals
We are Regeneron a leading science-based biopharmaceutical company dedicated to transforming lives through ground-breaking medicines. Our mission is to address high unmet medical needs across a range of therapeutic areas including ophthalmology oncology cardiovascular allergic inflammatory infectiou...
Clinical Development Medical Director- Nuclear Med...
Novartis
Job Description Summary#LI-HybridLocation: London United Kingdom or Dublin Ireland; Barcelona SpainAt Novartis were reimagining medicineand as Clinical Development Medical Director Nuclear Medicine youll be at the forefront of that mission. This is your opportunity to shape the future of oncology a...
Operations Assistant
Machine Medicine Technologies
About UsWe are a med-tech company leveraging cutting-edge AI to build scalable regulatory-grade tools for video-based motor assessments. As part of our growing technical team were looking for a versatile and driven Machine Learning Engineer to help build and maintain a robust framework for developin...
Clinical Trial Coordinator Cambridge
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthi...
Director, Clinical Pharmacology
Recursion
Your work will change lives. Including your own.The Impact Youll MakeYou will join an innovative and passionate clinical development team dedicated to improving the lives of patients suffering from devastating diseases. You will lead the innovative clinical pharmacology and pharmacometrics strategy...
Director, Clinical Pharmacology
Recursion
Your work will change lives. Including your own.Please note: Our offices will be closed for our annual winter break from December 22 2025 to January 2 2026. Our response to your application will be delayed.The Impact Youll MakeYou will join an innovative and passionate clinical development team dedi...
Director, Clinical Pharmacology
Recursion
Your work will change lives. Including your own.The Impact Youll MakeYou will join an innovative and passionate clinical development team dedicated to improving the lives of patients suffering from devastating diseases. You will lead the innovative clinical pharmacology and pharmacometrics strategy...
Sr Manager, Regulatory Affairs
Gilead Sciences
At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...
Medical Writer
Idibu
Medical Writer Oncology Central London Were looking for an experienced Medical Writer to join a growing drug development company based in central London focused on advancing innovative oncology treatments. This is an exciting opportunity to be part of a small agile and collaborative team working a...
Associate Clinical Development Medical Director (i...
Novartis
Job Description SummaryLocation: London United Kingdom or Dublin Ireland Role type: Permanent and Hybrid Working LI-HybridStep into a role where your clinical expertise will shape the future of global healthcare innovation. As an Associate Clinical Development Medical Director (IB) youll be at the h...
Global Program Clinical Head Renal
Novartis
Job Description SummaryThe Global Program Clinical Head (GPCH) is the global clinical leader responsible for one or more clinical programs across indications involving one or multiple compounds. The GPCH owns the risk benefit assessment for the program(s) and as the leader of Global Clinical Team(s)...
Medical Affairs Associate
Idibu
CK Group are recruiting for a Medical Affairs Associateto join a company in the pharmaceutical industry on a contract basis for 12 months. Salary: From 14.68 to 19.15 per hour dependant upon experience Medical Affairs Associate Role:Negotiate and obtain fully executed contracts as well as contract a...
Regulatory Affairs Director
Astrazeneca
Would you like to apply your Regulatory Affairs strategy expertise and passion to make an impact in a company that follows the science and turns ideas into life changing medicinesAt AstraZeneca we do this with the upmost integrity even in the most sophisticated situations because we are committed to...