Regulatory Documents Jobs in UK

The Role:The Associate Director CMC Regulatory Science-International will be based at the Harwell UK site and as part of a team be responsible for preparing and overseeing CMC and Quality related agency correspondence and regulatory applications as well as govern CMC submissions and regulatory compl...

The RoleJoining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is strengthening its presence in London a global center of science and innovation. Our team drives c...

The Associate Director (AD) Biostatistics leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions...

About Summit:Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life increasing potential duration of life and resolving serious unmet medical needs. At Summit we believe in building a team of world class professionals who are passionate a...

Nalco Water an Ecolab Company isseekingan experienced and motivated Pre-sales Engineerto join our innovation efforts and support our customers in the Global High Tech (GHT).We are seeking a candidate with a strong technical background who is hands-onideallywithpractical field/application experience...

Location: Remote candidates must be based in what of the selected locations.Join IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to...

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 and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to...

Come Build Your Career at Aecon!As a North American leader in infrastructure development Aecon is safely and sustainably building what matters for future generations to thrive! We lead some of the most impactful infrastructure projects of our generation at the forefront of transformational change in...

Come Build Your Career at Aecon!Aecon delivers some of the most complex and impactful infrastructure projects from transformative transportation networks to critical energy industrial and nuclear programs. The projects we build connect communities and power future generations. With deep roots in No...

We are seeking a detail-oriented and highly organized Nonclinical Regulatory Documentation Specialist to support the quality control preparation and management of nonclinical regulatory documents. This role plays a critical part in ensuring submission readiness for DMPK and Toxicology reports contri...

Do you have a passion for scientific writing and clinical research Then join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick-starting a global career in clinical trials.Fortrea Clinical Pharmacology Services (CPS) supports the earliest and most cri...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin us as a Medical Director M-SERM - And lead our efforts in medical safety evaluation and risk management.What Youll Do: Maintain understanding of methods for recording time spent on project and administrative tasks expen...

Job Title: Clinical Study Administrator Introduction to role: Are you ready to turn meticulous study coordination into real-world impact for patients Do you thrive on bringing order to complexity and keeping multi-site studies inspection-ready As a Clinical Study Administrator you will be a core mem...

ROLE SUMMARYThe Global Development Lead (GDL) Internal Medicine RU (IMRU) will be the thought leader driving clinical research for the expanding area of cardiometabolic diseases at Pfizer. The candidate will be responsible for creating the overarching strategy for early clinical development programs...

Fortrea is looking for an experienced clinical operations professional to join our team as Site Navigator II (remote) with a strong focus on clinical trial startup activities and in-house CRA responsibilities. This role is ideal for someone with solid startup expertise who is ready to take ownership...

Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONIf 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 col...

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...

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights faster breakthroughs and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A future in which diseases are cur...

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights faster breakthroughs and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A future in which diseases are cur...

Job Title: Transaction & Position Reporting Policy AssociateDivision: Enforcement Market OversightDepartment: Market OversightSalary: National (Edinburgh and Leeds) ranging from 43100 to 54000 and London from 47300 to 60000 (salary offered will be based on skills and experience)This role is graded a...