Regulatory Documents Jobs in UK
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Senior Epidemiologist (oncology, Breast Cancer, Rw...
Iqvia
This is a homebased position. Candidates can be located anywhere within one of the countries listed in the job ad. Candidates must have a permanent right to work in a country they apply for.Join IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring toget...
Clinical Study Coordinator
Idibu
CK Group are recruiting for a Clinical Study Coordinator to join a company in the pharmaceutical industry on a contract basis for 12 months. Salary: 14.68 to 19.39 per hour PAYE Clinical Study Coordinator Role:Negotiate and obtain fully executed contracts as well as contract amendments and track tri...
Clinical Study Coordinator
Idibu
CK Group are recruiting for a Clinical Study Coordinator to join a company in the pharmaceutical industry on a contract basis for 12 months. Salary: 14.68 to 19.39 per hour PAYE Clinical Study Coordinator Role:Negotiate and obtain fully executed contracts as well as contract amendments and track tri...
Regulatory Professional
Arxada
Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies in-depth regulatory know-how manufacturing and process development help our customers to safeguard nutrition health and infrastructure efficiently through chemistry and biotechnology that enhanc...
(senior) Clinical Development Director Cv
Novartis
Job Description SummaryThe *Senior Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As a Senior CDD in t...
Msat Director Drug Product
Summit Therapeutics Sub
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...
Medical Writer Iii, Regulatory Medical Writing, X-...
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Research Scientist (pi) Bioanalytical
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThis is a fully remote role supporting one of our key customers. We welcome applicants from all locations within the UK.TThermo Fishers clinical research business is a leading global contract research organization and world...
Associateprincipal Medical Writer
Trilogy Writing And Consulting
Senior/Principal Medical Writer Remote/Hybrid/In Office - UKTrilogy Writing & Consulting AnIndegeneCompanyis currently looking to hire Senior/PrincipalMedical Writers (f/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical indus...
Sr Associate Regulatory Affairs Cmc (x2)
Amgen
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...
Associate Director, Medical Monitor, Vaccines
Pfizer
ROLE SUMMARYThe clinician medical monitor may contribute towards providing medical and scientific expertise and oversight for Clinical Trials.The clinician medical monitor may be required to design a development strategy for multiple protocols designed to obtain worldwide approval for a compound or...
Associate Director, Medical Monitor, Vaccines
Pfizer
ROLE SUMMARYThe primary purpose is to serve as a Clinician within a Pfizer vaccine development program. This role may serve as a clinical lead for one or more studies within a clinical program and works closely with the global clinical program lead who is ultimately responsible for execution of the...
Quality Systems Specialist Document Control
Stryker
Work Flexibility: HybridJoin our Belfast team as a Quality Systems Specialist - Document ControlPosition Summary:The Document Control Specialist is responsible for managing organizing and maintaining controlled documents to ensure compliance with FDA regulations ISO 13485 and company quality managem...
Medical Writer Iii, Ai-assisted Operations
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Sr. Analyst, Medical Writing, Ai-assisted Operatio...
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Medical Writer Iii, Ai-assisted Operations
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...