Clinical Research Jobs in Prague
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Market Accessproduct Specialist
Iqvia
About the RoleWe are looking for a Market Access / Product Specialist to bridge the gap between business regulation and product development. This is a unique hybrid role combining product thinking with strong analytical and domain expertise in market access pricing or healthcare-related environments...
Lead Developer
Iqvia
Lead Developer / Engineering Team Lead (Backend Focus)About the RoleWe are looking for a hands-on Lead Developer to guide a small high-performing engineering team while driving the evolution of our product platform. This role combines technical leadership architecture ownership and team management w...
Qa Responsible Person (gdp)
Tfs Healthscience
Aout this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (FS...
Clin Ops Manager
Iqvia
Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential Functions Manage staff in accordance with organizations policies and applicable regulations. Responsibi...
Investigator Payments Analyst
Iqvia
PurposeThe Investigator Payments Analyst is accountable for budget planning analytics and payment execution in a direct country or extended country group (OPC and satellite countries) in close collaboration with the SSO Study Start-Up Managers SSO Clinical Project Managers and SSO Contracting Specia...
Study Start Up Manager (ssum) Czech
Iqvia
Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.Essential FunctionsOversee the execution of Site Activat...
Sso Site Partnership Manager, Emea Cze
Novartis
Job Description SummaryThe SSO Site Partnership Manager optimizes the cooperation with selected trial sites considered key accounts for Novartis with huge potential to significantly contribute to the portfolio execution aiming to improve performance in clinical studies regarding patient numbers time...
Research Physician (per Diem)
Thermo Fisher Scientific
Work ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionConducts all clinical trials (studies) according to ICH GCP local regulations study protocol and company processes. Ensures the medical wellbeing and safety of the participants through the safe performance and execution of the studies. M...
Sales Op. Manager
Iqvia
Job OverviewDrives and implements the sales operations infrastructure across a large market or sales operation specialty(s) across a large region.Essential Functions Drives and leads the effective implementation of sales operations initiatives such as opportunity management tracking and forecasting...
Medical Sales Representative, Czech Republic
Iqvia
IQVIA is a global leader in human data science partnering with life sciences organizations to improve patient outcomes and accelerate innovation. We are building a team of Medical Sales Representatives to sell to cardiologists and other specialists.Territory- Praha and Plzeň and surrounding areaKey...
Clinical Research Nurse (per Diem)
Thermo Fisher Scientific
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 Nurse (per Diem)
Thermo Fisher Scientific
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...
Clinical Research Coord
Fox Chase Cancer Center
Your Tomorrow is Here!Temple Health is a dynamic network of outstanding hospitals specialty centers and physician practices that is advancing the fight against disease pushing the boundaries of medical science and educating future healthcare professionals. Temple Health consists of Temple University...
Clinical Trial Administrator
Novo Nordisk
Clinical Trial AdministratorResearch & DevelopmentCzech RepublicReady to help deliver clinical trials that bring life-changing treatments to patients Your precision and dedication can turn scientific breakthroughs into real-world impactso patients benefit sooner.Your new roleAs a Clinical Trial Adm...
Experienced Clinical Research Associate Sponsor De...
Iqvia
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...
Local Trial Manager Sponsor Dedicated
Iqvia
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical the team provides the opportunity to work with one single client and to manage clinical research projects in different therapeutic areas....
Regional Sales Manager, Specialty Medicines (czech...
Iqvia
IQVIA is recruiting a Regional Sales Manager to lead commercial activity for a portfolio of specialty medicines on behalf of one of our pharmaceutical partners. This role provides the opportunity to take responsibility for multiple countries operating within a complex matrix environment and working...
Regulatory Affairs Regional Dossier Publisher
Msd
Job DescriptionThe Regional Dossier Publisher (RDP) will work within the Global Regulatory Affairs and Clinical Safety (GRACS) organization in the EUEEMEA Regulatory Operations (RRO-EUEEMEA) Team.The RDP is responsible for publishing key regulatory submissions in the region and supporting the publis...
Regulatory Affairs Operations
Msd
Job DescriptionThe Regulatory Affairs Operations will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and supporting business pro...
Regulatory Affairs System Process & Innovation
Msd
Job DescriptionThe Regulatory Affairs - System Process & Innovation will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and sup...