Clinical Research Associate Manager Jobs in Czech Republic

Job Description SummaryJob Title: Senior Clinical Research Associate (CRA)#LI-HybridPrimary Location: Prague Czech RepublicRelocation Support: This role is based in Prague. Novartis is unable to offer relocation support: please only apply if accessible.Drive clinical trials forward where it matters...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials ac...

No Relocation Assistance OfferedJob Number#173263 - Prague Prague Czech RepublicWho We AreColgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care Personal Care Home Care Skin Care and Pet Nutrition. Our products are trusted in more ho...

Job DescriptionClinical Research ManagerThe OpportunityExciting opportunity to join an innovative and trusted Global biopharmaceutical companyPermanent Full-time opportunityFlexible and hybrid working arrangementsThe Clinical Research Manager (CRM) will primarily accountable for the end-to-end perfo...

Work ScheduleOtherEnvironmental ConditionsOffice Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Will work with hazardous/toxic materialsJob DescriptionConducts clinical studies according to Czech legislation and ICH regulations and...

Work ScheduleOtherEnvironmental ConditionsOffice Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Will work with hazardous/toxic materialsJob DescriptionConducts multiple ongoing clinical trials of varying size and complexity involvi...

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements i.e. Good Clini...

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements i.e. Good Clini...