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...

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 clarify clinical trial regulatory pathways, share lessons...

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...

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...

**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...

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 a home-based role seeks an associate manager to contribute to study strategy development and collaboration with global teams. You will perform data mining, analysis, and form recommendations for country, site, or enrollment planning, coordinating with IQVIA experts to support opportunities and bids.The role requires 2–3 years of clinical research...

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 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...

Overview As a Contracts Manager within the IQVIA US Contracting Center (USCC), you will review, draft and/or redline contracts within the U.S. business unit with a focus on IQVIA’s commercial services (data, analysis services, consulting, technology). Overview As a Contracts Manager within the IQVIA US Contracting Center (USCC), you will review, draft...

IQVIA Laboratories in Buenos Aires, Argentina seeks a Quality Control Analyst to ensure study setup quality and adherence to procedures. Under guidance, you’ll QC lab documents and database configurations, support process excellence, and maintain high quality standards across IQVIA.You will collaborate with Set-up Managers and cross-functional teams to...

IQVIA is a leading global provider of clinical research services and healthcare insights. The role leads site activation and maintenance across studies, guiding regulatory strategies and execution for multi-protocol programs.You will coordinate with cross-regional teams, ensure regulatory compliance, review documentation, and support business development...

Buenos Aires, Argentina | Full time | Home-based | R1558401 **We are seeking Quality Control Analyst to join IQVIA Laboratories at Buenos Aires, Argentina.**: - We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and...

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...

We are seeking Operational Quality Specialist to join IQVIA Laboratories at Buenos Aires, Argentina. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary: Support and enhance...

IQVIA Laboratories in Buenos Aires, Argentina is seeking an Operational Quality Specialist to support and enhance global laboratory quality and technical systems, overseeing assay quality control processes and proficiency testing.You will collaborate across laboratory, scientific, data management, vendor and management teams to ensure consistent quality...

IQVIA is seeking a Safety Data Reviewer to review, assess and process safety data across service lines, ensuring regulatory SOP adherence with guidance from senior operation team members.This tri-lingual role requires fluency in English, Spanish, and Italian, and offers a 100% remote work arrangement, with health benefits and performance bonus opportunities....

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine: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...

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...