Company: IQVIA, Inc.
The Global Clinical Lead/Study Lead – Country Operations – (SLCO) serves as the primary contact for the Country Operations Management (COM) team on a global study level, collaborating closely with the Clinical Project Lead (CPL) and other functional stakeholders. This role acts as the global representative for COM, facilitating communication between in-country teams and the [...]Read More... from Global Clinical Lead – Sponsor Dedicated See details
We are seeking a highly skilled and experienced Clinical Programmer (Data Visualization Expert) to join our FSP Team. Key Responsibilities: Develop, test, and validate clinical data programs and applications. Ensure compliance with CDISC SDTM standards for clinical data. Utilize visualization tools such as Sport fire or other similar tools to create insightful data visualizations. Write [...]Read More... from Senior Clinical Programmer (Python Expert) See details
The team & the company IQVIA 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 data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare [...]Read More... from Medical Writer (Consultant for HTA) – Lisbon or Athens See details
This will be an initial 6 months Fixed Term Contract with possible extension. Immediate joiners preferred. Primary Responsibility Ensure ICSR case processing and related activities comply with regulatory requirements, company procedures, and PV agreements at local, regional, or global levels. Inbound & Outbound ICSR Case Management Handle receipt, assessment, and processing of safety information from [...]Read More... from Pharmacovigilance Specialist See details
Job Overview: As Biostatistics Director, you will liaise with cross-functional teams to drive the quality statistical planning, analysis, and reporting in support of pharmaceutical development and regulatory submissions. Serve as a resource for the department, ensuring scientific integrity and regulatory compliance in the application of statistical methodology to clinical trials. Participate as lead statistician on [...]Read More... from Director, Biostatistics (FSP – Permanent Homebased) See details
Job Overview: As Associate Director, you will liaise with cross-functional teams to drive the quality statistical planning, analysis, and reporting in support of pharmaceutical development and regulatory submissions. Serve as a resource for the department, ensuring scientific integrity and regulatory compliance in the application of statistical methodology to clinical trials. Participate as lead statistician on [...]Read More... from Associate Director, Biostatistics (FSP – Permanent Homebased) See details
Job Overview Manage medium to large multi-regional Connected Devices projects that are stand-alone or full-service in scope, across all clinical trial phases. Ensure all project work is completed to the sponsor’s satisfaction, on time and within budget and in accordance with policies and procedures. Essential Functions Plan, initiate, execute, control, and deliver projects in accordance [...]Read More... from Connected Devices – Clinical Project Manager See details
Advanced AI, IQVIA Applied Science, Real World Solutions London/EU/Hybrid/Remote Our Advanced AI Group is a dynamic, rapidly expanding team of collaborative and innovative AI researchers within the IQVIA Applied Science organization. The team is focused on pushing the boundaries of foundation models and autonomous systems, with recent contributions to the field, including publications at ICML [...]Read More... from AI Scientist – Agentic AI / Gen AI / LLM See details
Why IQVIA This role will be dedicated to one of IQVIA’s largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech [...]Read More... from Senior Statistical Programmer (Remote – Permanent Homebased) See details
Job Overview Manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer’s satisfaction. Provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs. Provide leadership to the team in the area of coding, project planning and execution, financial management, [...]Read More... from Senior Clinical Data Coder – Sponsor-dedicated, Homebased (multiple locations in EMEA) See details
