Regulatory Documents Jobs in UK

The RoleLeading our Health & Safety team youll be responsible for the systems processes and behaviours that make sure everyone leaves our sites across London safely at night. Youll be our point person on legislation changes a great coach that helps teammates improve and the guardian of the measures...

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...

DepartmentFinancial PlanningEmployment TypePermanent - Full TimeLocationCity LondonWorkplace typeHybridCompensation65000 - 75000 / year Key Responsibilities Skills Knowledge and Expertise About Moore Kingston Smith At Moore Kingston Smith we believe in the p...

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...

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...

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)...

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...

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...

Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks) United Kingdom or Dublin IrelandInternal Job Title: Global Program Regulatory Associate DirectorWe are looking for an experienced and proactive Senior Global Program Regulatory Manager to join our Global Re...

Align with the Director to enhance the roadmap and develop the action plan to implement AbbVies Patient Inclusion strategy across the portfolioCollaborate with cross-functional partners to identify process improvements to disease area strategies and clinical trial lifecycle to increase representativ...

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...

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...

Job Title Enforcement and Market Oversight Litigations LawyerDivision - Enforcement and Market OversightDepartment Wholesale and Unauthorised Business InvestigationsTeam Wholesale 2Salary National ranging from 79400 to 100000 and London from 87300 to 123500 (Salary offered will be based on skill...

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee youll be part of a continually growing organization working alongside e...

Are you ready to turn ideas into life-changing medicines At AstraZeneca we are driven by the potential of science to address unmet patient needs globally. Our vision is to push the boundaries of science redefining the practice of medicine and ultimately eliminating diseases like cancer respiratory c...

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee youll be part of a continually growing organization working alongside e...

The PrimeVigilance Senior Medical Writer role offers a unique opportunity to further develop your career in the field of drug safety. You will be working in an international team of experienced aggregate report writers contributing to further departmental growth. Key ResponsibilitiesIndependent auth...

CK Group are recruiting for a Principal Scientist PKPD to join a global pharmaceutical company on a contract basis initially for 12 months. Salary: 35.20 Per hour (PAYE) / 47.92 (Umbrella) - flexible for experienced candidates. Principal Scientist PKPD Role:Participate in the developmen...

Job Description SummaryLOCATION: London United Kingdom or Dublin Ireland or Basel SwitzerlandROLE TYPE: Hybrid Working #LI-HybridStep into a role where your clinical expertise can shape the future of neuroscience. As Associate Clinical Development Director youll be at the forefront of global clinica...

About LabCorp:As a leading contract research organization LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment clinical trial testing and clinical trial management services. Together with our clients we support t...