Iqvia
Job OverviewPerform 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 (sele
Job OverviewPerform 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 (sele
Associate Regulatory & StartUp ManagerClinical Operations Regulatory & Site ActivationLocation: Flexible / officebased depending on project needsTravel: Occasional travel may be requiredContract Length: 4-6 monthsAre you looking to take the next step in your Regulatory & StartUp care
Associate Regulatory & StartUp ManagerClinical Operations Regulatory & Site ActivationLocation: Flexible / officebased depending on project needsTravel: Occasional travel may be requiredContract Length: 4-6 monthsAre you looking to take the next step in your Regulatory & StartUp care
Regulatory & StartUp ManagerClinical Operations Regulatory & Site ActivationLocation: Flexible / officebased depending on project needsTravel: Occasional travel may be requiredContract Length: 4- 6 monthsAre you an experienced Regulatory & StartUp professional looking to lead complex
Regulatory & StartUp ManagerClinical Operations Regulatory & Site ActivationLocation: Flexible / officebased depending on project needsTravel: Occasional travel may be requiredContract Length: 4- 6 monthsAre you an experienced Regulatory & StartUp professional looking to lead complex
Clinical Supply Chain ManagerFull home-based Job OverviewThe Clinical Supply Chain Manager is responsible for the strategic planning and execution of new clinical trial supply chains. This involves the ability to interpret a clinical trial protocol in conjunction with other key study
Clinical Supply Chain ManagerFull home-based Job OverviewThe Clinical Supply Chain Manager is responsible for the strategic planning and execution of new clinical trial supply chains. This involves the ability to interpret a clinical trial protocol in conjunction with other key study
We are seeking highly experienced Python Programmer candidates with minimum 6 years of relevant experience Strong proficiency in Python programming preferably with handson experience in PySpark and PandasHandson experience in Data VisualizationSolid working knowledge of SQLExperience
We are seeking highly experienced Python Programmer candidates with minimum 6 years of relevant experience Strong proficiency in Python programming preferably with handson experience in PySpark and PandasHandson experience in Data VisualizationSolid working knowledge of SQLExperience
We are looking for a skilled PatientLevel Data (PLD) Consultant with 3 years of handson experience in patientlevel analytics and SQL along with a solid understanding of segmentation targeting and sales force effectiveness (SFE). The role involves working with largescale healthcare dat
We are looking for a skilled PatientLevel Data (PLD) Consultant with 3 years of handson experience in patientlevel analytics and SQL along with a solid understanding of segmentation targeting and sales force effectiveness (SFE). The role involves working with largescale healthcare dat
The team & the companyIQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics transformative technology big
The team & the companyIQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics transformative technology big
Iqvia
Quieres iniciarte en el mundo de la visita médica dentro de la industria farmacéuticaIQVIA es líder mundial en el uso de datos tecnología analíticas avanzadas y experiencia humana para ayudar a sus clientes a impulsar el cuidado de la salud. Junto a las empresas a las que prestamos se
Quieres iniciarte en el mundo de la visita médica dentro de la industria farmacéuticaIQVIA es líder mundial en el uso de datos tecnología analíticas avanzadas y experiencia humana para ayudar a sus clientes a impulsar el cuidado de la salud. Junto a las empresas a las que prestamos se
IQVIA es líder mundial en el uso de datos tecnología analíticas avanzadas y experiencia humana para ayudar a sus clientes a impulsar el cuidado de la salud. Junto a las empresas a las que prestamos servicios estamos habilitando un sistema de salud más moderno más efectivo y más eficie
IQVIA es líder mundial en el uso de datos tecnología analíticas avanzadas y experiencia humana para ayudar a sus clientes a impulsar el cuidado de la salud. Junto a las empresas a las que prestamos servicios estamos habilitando un sistema de salud más moderno más efectivo y más eficie
This opportunity is available in multiple locations across Europe (within the European Union and the UK). Please dont hesitate to apply even if you dont see your preferred location listed. The role can be hybrid or fully homebased. Please submit your CV in English.Principal COA Implem
This opportunity is available in multiple locations across Europe (within the European Union and the UK). Please dont hesitate to apply even if you dont see your preferred location listed. The role can be hybrid or fully homebased. Please submit your CV in English.Principal COA Implem
We are recruiting an awesome team of German language speakers to join us at our Madrid Production Hub office working on remote! We are looking for German native speakers.. diversity is our way of life!!Your primary focus will be to be responsible for building up and maintaining update
We are recruiting an awesome team of German language speakers to join us at our Madrid Production Hub office working on remote! We are looking for German native speakers.. diversity is our way of life!!Your primary focus will be to be responsible for building up and maintaining update
Job OverviewLead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work clinical study management and project deliverables are on time and is in accordance with SOPs policies and Good Clinica
Job OverviewLead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work clinical study management and project deliverables are on time and is in accordance with SOPs policies and Good Clinica
Opportunity in a dynamic multisponsor environment - we are looking for experienced CRAs for our Site Management Team in Poland!ResponsibilitiesPerform site monitoring visits (selection initiation monitoring and close-out visits) in accordance with contracted scope of work and regulato
Opportunity in a dynamic multisponsor environment - we are looking for experienced CRAs for our Site Management Team in Poland!ResponsibilitiesPerform site monitoring visits (selection initiation monitoring and close-out visits) in accordance with contracted scope of work and regulato
Iqvia
IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry dedicated to creating intelligent connections that deliver unique innovations and actionable insights. We help to speed drug development ensure pr
IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry dedicated to creating intelligent connections that deliver unique innovations and actionable insights. We help to speed drug development ensure pr
Job OverviewServe as the liaison between Records Management and user departments regarding Trial Master Files (TMF). Apply Records Management expertise to provide project related assistance across complex and multiple project(s) sites and project teams. Ensure all work is conducted in
Job OverviewServe as the liaison between Records Management and user departments regarding Trial Master Files (TMF). Apply Records Management expertise to provide project related assistance across complex and multiple project(s) sites and project teams. Ensure all work is conducted in
Job OverviewThe Associate Director PSCS Finance Operations is responsible for the strategic direction oversight and delivery of complex projects and/or multiproject programs within the PSCS Finance organization. This role ensures that project deliverables are completed on time within
Job OverviewThe Associate Director PSCS Finance Operations is responsible for the strategic direction oversight and delivery of complex projects and/or multiproject programs within the PSCS Finance organization. This role ensures that project deliverables are completed on time within
Location:South Africa/KenyaBusiness Unit:IQVIA Real World EvidenceReporting to:AssociatePrincipalRole OverviewTheStudyManager isresponsible forthe operational planning coordination and delivery ofReal WorldEvidence (RWE) observational andglobalhealth projects across SubSaharan Africa
Location:South Africa/KenyaBusiness Unit:IQVIA Real World EvidenceReporting to:AssociatePrincipalRole OverviewTheStudyManager isresponsible forthe operational planning coordination and delivery ofReal WorldEvidence (RWE) observational andglobalhealth projects across SubSaharan Africa
Job OverviewLead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work clinical study management and project deliverables are on time and is in accordance with SOPs policies and Good Clinica
Job OverviewLead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work clinical study management and project deliverables are on time and is in accordance with SOPs policies and Good Clinica
Job Overview:The Customer Service Client Support Specialist plays a key role in supporting our Sales Team and ensuring exceptional service for our Enterprise client accounts. You will collaborate closely with Account Managers and Business Development Directors to streamline sales pro
Job Overview:The Customer Service Client Support Specialist plays a key role in supporting our Sales Team and ensuring exceptional service for our Enterprise client accounts. You will collaborate closely with Account Managers and Business Development Directors to streamline sales pro
Job OverviewIndividual contributor who is fully proficient in applying subject matter knowledge for a professional discipline. Works under limited supervision.Essential Functions Acts as a Regulatory Team Leader on more complex projects which may include technical writing; Prepares an
Job OverviewIndividual contributor who is fully proficient in applying subject matter knowledge for a professional discipline. Works under limited supervision.Essential Functions Acts as a Regulatory Team Leader on more complex projects which may include technical writing; Prepares an