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Job OverviewPerform monitoring and site management work for a variety of protocols, site and therapeutic areas.Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference...

Popis pracovnej ponuky Mzda Nástupná mesačná mzda pri úväzku 38,75 hod./týž.: 1.570 € Nástupná mesačná mzda pri úväzku 35 hod./týž.: 1.418 € Nástupná mesačná mzda pri úväzku 30 hod./týž.: 1.215 € Nástupná mesačná mzda pri úväzku 25 hod./týž.: 1.013 € Samozrejmosťou ku mzde sú všetky zákonné príplatky. Zmluvne...

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. Maintains clinical oversight and quality on the studies...

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 2,700 clinical trials across 100+ countries in the last 5 years.As part of our...

TFS 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 (FSP) solutions. Join Our Team as a Freelance Senior Clinical Research...

Work ScheduleOtherEnvironmental ConditionsSome degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job 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...

Operátorka výroby – výroba plastových výliskovMzda: od 33 000 Kč mesačnePracovný pomer: Hlavný pracovný pomerPracovná doba: Dvojzmenná prevádzka, do budúcna možnosť nočných zmien.Práca spočíva v obsluhe výrobných zariadení určených na výrobu plastových výliskov. Súčasťou pracovnej náplne je odoberanie hotových...

Firma ATMSolutions poszukuje pracownika na stanowisko Operatora maszyn CNC. Osoba Na Tym Stanowisku Będzie Odpowiedzialna M.in. Za • Ustawianie i obsługę obrabiarek skrawających CNC • Wykonywanie detali zgodnie z dokumentacją • Przygotowanie maszyn do pracy oraz ich obsługa - programowanie, przezbrajanie Oczekujemy • min. 2 letniego...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionVedoucí týmu zdravotních sester(interní název pozice: Supervisor Nursing)Staňte se součástí klinického výzkumu, který přináší pacientům přístup k inovativní léčběDo našeho týmu hledáme zkušenou zdravotní sestru nebo zdravotnického pracovníka se...

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 2,700 clinical trials across 100+ countries in the last 5 years.As part of our...

CRA II - SCRA I - CzechiaSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team...

CRA IISyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug...

Du bist Gamer, hilfst gerne anderen und sprichst fließend Deutsch und Englisch ? Wir suchen einen deutsch- und englischsprachigen E-Mail-Support-Spezialisten für ein internationales Gaming-Support-Team in Sofia, Bulgarien . In dieser Position unterstützt du Spieler per E-Mail bei Fragen und Problemen und trägst dazu bei, ihnen ein reibungsloses und...

The ESO Quality Senior Specialist is responsible for the full quality lifecycle management of an assigned product portfolio and independent Quality Assurance oversight of external suppliers.The role leads complex quality topics, identifies and manages quality risks, drives improvements within the Quality Management System, and acts as a senior Quality expert...

Informed Consent Specialist IICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global...

DescriptionAbout the RoleThe Regulatory Start-Up Lead (RSL) are responsible for the planning, preparation, and review of country- and site-level ethics and regulatory authority submissions during the start-up phase of clinical trials, and, where applicable, throughout maintenance and close-out. They ensure that all submissions comply with ICH-GCP guidelines...