Please do not apply if you are not located in UK / EUAbout the jobAbout FreyrFreyr is a fast-growing, innovative company specializing in providing end-to-end regulatory solutions and services for the Life Sciences industry. With a commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navigating the complexities of regulatory compliance.Why Freyr?At Freyr, we believe in fostering a collaborative and dynamic work environment that empowers our team to make a real impact. As we expand our footprint to Warsaw, Poland, we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services.Join Our Team:If you're ready to embark on a journey of growth and innovation, connect with us to explore the exciting opportunities awaiting you at Freyr's new chapter in Warsaw, Poland. Together, we can shape the future of regulatory solutions.Title: Regulatory Affairs Manager Clinical TrialsLocation: UKKey Skills: EU-CTR / CTIS, MHRA, ARSAC submissions, UK Submission, IRAS, UK Study Start upDescriptionExperience with leading MHRA, REC and study-wide review submissions under the combined review in the new IRASExperience in UK study start-up:ARSAC submissionsPharmacy Assurance applicationsRadiation Assurance applicationsHighly preferable:Experience in UK study start-up:Experience with Self-managed Radiation assuranceOptional (plus):Specialized knowledge in UK study start-up:CRN network (National Institute for Health Research (NIHR) Clinical Research Network) submissionsCommunicating amendments to sitesSeniority levelMid-Senior levelEmployment typeFull-timeJob functionOtherIndustriesPharmaceutical Manufacturing #J-18808-Ljbffr