iqvia

IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating clinical site contracts and budget templates.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough...

IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough...

Senior Clinical Research Associate (Sr CRA 3) – ArgentinaIQVIA Biotech, a full-service CRO, is seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team in Argentina. In this role you will independently manage and monitor clinical trial sites to ensure studies comply with protocols, Good Clinical Practice...

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team in...

IQVIA Biotech is hiring for Sr. Site Contracts Associate in with 3-5 years experience negotiating clinical site contracts and budget templates. Grant Plan a plus.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help...

Buenos Aires, Argentina | Full time | Home-based | R1550155 Key Responsibilities - Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. - Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level. - Engage directly with clients to...

Job Overview Direct 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. Essential Functions • Oversee the execution of Site Activation (including pre-award/bid defense activities)...

IQVIA is seeking a Leader of the Centralized Monitoring team to partner with the project and clinical leads to achieve delivery objectives, while optimizing speed, quality and cost in line with IQVIA SOPs.This role manages study metrics, mentors staff, supports monitoring strategy, and ensures audit-ready documentation across global projects, requiring...

IQVIA is seeking a candidate to oversee patient recruitment and retention operational plans for small to mid-size studies. You willCoordinate with sponsors and project teams to implement tactical plans and monitor impacts.You will collaborate with internal teams and external providers to deliver recruitment tactics, represent IQVIA at meetings, train CRAs...

IQVIA in Esquel, Argentina is seeking a detail-oriented support professional to provide incident and service request support, applying knowledge of IQVIA products and technical expertise to deliver effective technology services.You will participate in problem identification, system architecture discussions, hardware/software specifications, design,...

IQVIA is seeking a Senior Clinical Research Associate to lead planning, execution, and management of clinical trials. This role ensures data integrity, regulatory compliance, and successful trial outcomes across sites.The candidate will monitor sites, support recruitment planning, train site staff, and track regulatory submissions while collaborating with...

IQVIA is seeking a Contracts Manager to review, draft, and redline contracts for the US Contracting Center with a focus on data, analysis services, and technology. The role emphasizes independent handling of high-volume reviews and collaboration with cross-functional teams to ensure alignment with IQVIA objectives.Ideal candidates have 3–4 years of...

IQVIA in Argentina seeks a Site Activation Manager to direct and manage the execution of regulatory, ethics, contracting, and site activation activities for clinical studies at the local level.You will oversee Start Up and Lifecycle Maintenance, ensure alignment with project timelines, and maintain site activation plans while communicating with study teams...

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. Developing professional individual contributor who works...

Job Overview Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

IQVIA is seeking a Data Management Lead in Buenos Aires to independently manage end-to-end delivery of data management services across multiple global studies. You will provide leadership to the Clinical Data Management team, ensuring timely and quality deliverables while maintaining strong customer relationships. With 7 years of direct experience, including...

IQVIA is seeking a Clinical Lead to provide global study leadership across regional and global trials. You will partner with Project Leaders, sponsors, and cross-functional teams to deliver studies with quality, patient recruitment, site performance, and operational excellence.The role involves directing clinical delivery, guiding teams, ensuring regulatory...

IQVIA seeks a seasoned regul​atory/site-activation lead to direct delivery of activation, maintenance and regulatory activities for studies in Argentina. You'll oversee pre-award activities, budget and resources, ensuring regulatory compliance and successful study initiation.Work closely with Regulatory & Site Activation teams, study management, and...

Aspen Pharma busca un Analista de BI & SFE para sumarse al equipo de Cono Sur en Puerto Madero. El rol genera información estratégica para decisiones y optimiza la efectividad comercial mediante análisis de datos, indicadores y reportes automatizados.Se trabajará con IQVIA, Close Up y CRM para brindar soporte a Ventas, Marketing y Finanzas, generando...

IQVIA Biotech in Argentina is seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to independently monitor clinical trial sites, ensuring adherence to protocols, GCP, ICH guidelines, regulatory requirements and sponsor expectations.Responsibilities include site qualification/initiation, routine monitoring and closeout visits; training site...