iqvia

AnalystLevel: Early Talent (On Campus)As Analyst within IQVIA, our steadfast mission drives the acceleration of patients' treatment access through insightful data analysis. Our unique role enables precise deliveries for customers. Each Analyst contribution propels this mission—facilitating patient i

IQVIA is looking to appoint a Medical Advisor/Associate Medical Director to be part of our Medical Services team to deliver medical, clinical and scientific advisory expertise in clinical research studies. You will support compliance with protocol execution from a medical and scientific perspective.

The EDC Data Acquisition Expert performs activities relating to the definition and implementation of Clinical Electronic Data Capture tools (EDC) and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture. Activities are performed in close collabor

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, besse

Job OverviewConduct and/or support audits and report preparation/distribution, Support quality issues management, Customer Audit/ Regulatory Inspections hosting, Corrective and Preventative Action (CAPA) and Effectiveness Check (EC) plan review, approval and closure and Audit plan development. Provi

Job OverviewProvides administrative and/or technical support. Recruitment Process 第一轮：线上测评 完成指定的线上测试，用于初步筛选。 第二轮：业务面试 与业务部门进行面谈，深入了解您的专业背景与职位匹配度。 第三轮：结果通知 招聘团队将在流程结束后，正式告知最终结果。 Essential Functions• Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’

Job Overview Provides administrative and/or technical support. Recruitment Process 第一轮：线上测评 完成指定的线上测试，用于初步筛选。 第二轮：业务面试 与业务部门进行面谈，深入了解您的专业背景与职位匹配度。 第三轮：结果通知 招聘团队将在流程结束后，正式告知最终结果。 Essential Functions• Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors

Manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out. Work with study(ies)/program(

Scope of work:a) Support CIQ application for related commodity (eg: pregnancy kits, selected model of urine dipstick etc).b) Support to work with local vendor to study if other current restricted items (like parapak) can be exported and work on its exporting process.c) Support on the new (recently c

Job Overview Responsible for managing laboratory staff across a large department or multiple related departments. Assists with the administration of laboratory testing in accordance with applicable regulations governing clinical laboratories. Contributes to departmental strategy and drives achieveme

Job Overview Responsible for Project Management operational delivery. Serves as a key contact for internal and external business relationships. Manages the design and launch of non-standard, complex clinical research studies as assigned. Reviews processes and provides expertise to improve project ex

Essential Functions Codes data, as required, transforming incoming paper data from suppliers into electronic data files. Interprets written responses and enters them into electronic coding systems, allocating data to standard reference systems. Performs quality assurance on coded data to ensure it a

For our Hungarian office, IQVIA is looking to hire an Assoc CRA. Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) model gives you the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of

Essential Functions• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures

Advance level role Provide timely status updates including issues & risks to DM and DMLs as needed Act as the Point of contact for Clinical Data Manager, working pro-actively to identify risks and provide mitigations May communicate with the vendors to resolve reconciliation issues. Provide input to

Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical tea

Wat houdt de job in? Je behaalt salesdoelstellingen en verhoogt de brand awareness van het CVRM‑portfolio bij huisartsen in de regio Waasland – Vlaams‑Brabant. Je promoot de producten volgens de richtlijnen en ontwikkelt tactische plannen om de positionering te versterken. Je bouwt sterke relaties o

Are you looking for an opportunity as a Clinical Research Nurse? Do you want to work for an industry leading company. This is a part-time, freelance role to support a variety of clinical trials in Madrid on an ad hoc basis. We are looking for candidates with the following skills and experience: BS/B

Functie en context Voor een gespecialiseerd farmaceutisch bedrijf binnen vrouwengezondheid zoeken we een ervaren medisch afgevaardigde. Je promoot bij huisartsen geneesmiddelen en voedingssupplementen binnen domeinen zoals anticonceptie, menopauze, fertiliteit en zwangerschap. Je bent actief in de r

Job Overview Perform 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 maintenance activities