QUALITY INVESTIGATOR jobs in UNITED KINGDOM, United Kingdom #8

APRIL Hub Director (Principal Investigator), with on-going engagement with other researchers in the Hub as well as academic... Engineering was ranked 1st in Scotland and 3rd in the UK for quality and breadth of research. The ranking cited is based upon the...

but not limited to the development of Clinical trial reports (CTRs) Lay summaries of clinical trial results Investigator brochures... of your career - both now, and into the future. Our success depends on the knowledge, capabilities and quality of our people...

. Join us! What you will do Mentors and leads a team of Quality professionals and ensures quality deliverables, on time, and in compliance... and review of Quality Management Documents (SOPs, WIs, etc.) Supports the management of the vendor audit program as it relates...

protocol, investigator brochure, participant information and consent forms, budget, timelines, and safety reporting... documents to support a clinical trial. Identify quality risks and issues, respond to issues raised by project team and plan...

to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future...: The primary responsibilities of the Research Scientist will be to act as principal investigator on indirect treatment...

regulations and to apply them. Is responsible for the local compliance with the applicable quality referential and their evolution... for the update of the quality documentation related to PV. Provides his/her colleagues with these documents and explains them...

by having clear systems to ensure data integrity, quality control and evidence of protocol compliance 4. Ensure... with all necessary essential documentation, in preparation for pharmacy sign off by the Trial Chief Investigator b) Arrange...

on data management issues/ICF issues/ quality issues/ investigator site file (ISF) issues/site staff issues to develop... with clinical sites and KOLs globally. Lead Site/Investigator meetings and represent study team at industry conferences...

, policies, local regulatory requirements, ICH-GCP, etc. Complies with relevant training requirements. Contribute to quality... from local area about site/investigator selection in collaboration with the trial team, as required. Act as primary company...

on data management issues/ICF issues/ quality issues/ investigator site file (ISF) issues/site staff issues to develop... with clinical sites and KOLs globally. Lead Site/Investigator meetings and represent study team at industry conferences...

. Coordinate the TMF Quality Check (per Ipsen SOP) with the CRO/Ipsen to ensure the eTMF inspection readiness. Coordinate the... meetings (invitation/room booking/lunch order...) such as Investigator’s meeting, DRM & TFLs, Steering Committee, … Attend...

To generate consistently high-quality clinical documentation content, working across multiple accounts and projects seamlessly... documents e.g. investigator brochures, protocols, CSRs, briefing documents, meeting requests, CTD Clinical modules. Writes...

to support MoonLake’s development programmes. This includes (not limited to) clinical study protocols, investigator brochures... to ensure quality and accuracy within and between development documents. Lead the development of templates for core documents...

. You will maintain all files pertaining to the clinical trials, track study progress and ensure timely quality updates are provided... is completed correctly and within designated timelines. You will bridge the gap between the Principal Investigator and research...

laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve... of assigned studies Provides quality oversight to the Contract Research Organization (CRO) and of the CRO deliverables related...