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.Home Based role requiring experience with المزيد...

Contract Duration - 1 year.Position Overview:We are looking for a highly organized and proactive Event Logistics and Governance Coordinator to handle the planning execution and management of events logistics and governance processes.The ideal candidate will ensure compliance maintain المزيد...

Job OverviewProvide advanced technical expertise to develop and maintain programs to meet internal and external clients needs. Plan and lead the development of project-related solutions to the full scope of statistical programming tasks. Provide technical expertise to the Statistical المزيد...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc المزيد...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc المزيد...

Internal Job DescriptionJob 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.Home Based role r المزيد...

Associate Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studi المزيد...

Job OverviewCollaborate with pre and post award stakeholders to manage the coordination planning quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of smaller programs in their المزيد...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc المزيد...

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a health المزيد...

and quality data management products) to Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities and may provide leadership either in the role of the Lead Coder or in a specific CDM task (e.g. Data Operations Coordinator ( المزيد...

We currently offer an exciting opportunity as Manager Clinical Operations (m/w/d) to work in a sponsor dedicated setting with one key client home-based throughout Germany.In our Clinical Functional Service Partnership team we work in a close partnership with our key customers to deliv المزيد...

Associate Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studi المزيد...

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.Hybris role onsite 3 x a week in Athens. المزيد...

Job OverviewApply knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including safety aggregate reports literature surveillance signal management activities and benefit risk management documents.Essential Functions Serve as principal owner of المزيد...

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a health المزيد...

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. Support senior leadership on resourcing strategies and with local clients relationship.Essential المزيد...

OverviewIQVIA provides scientific solutions spanning clinical trials real world evidence and consulting in all areas of the drug product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the المزيد...

Job OverviewProvide management and service delivery excellence of (Clinical Event Validation and Adjudication) CEVA OGM (Oversight Group Management) projects as assigned by CEVA Management covering single or multiple CEVA-OGM functions with supervision from project oversight. Provide المزيد...

As a Senior Medical Review you will be part of a dynamic team working across multiple different therapy areas with some of the leading pharmaceutical companies. You will be reviewing documents for scientific accuracy against the applicable regional codes (ABPI EFPIA etc.). These docum المزيد...