iqvia

Essential Functions Review Requests For Proposal (RFP). Identify information for proposal text and budget development and work closely with proposal development team to prepare and finalize proposals. Prepare text and budget for proposals, rebids and related documents. Provide support and assistance

Only CVs/resumes in English will be considered Location: Remote / Home-Based (Mexico & Brazil) Language Requirement: Fluent English Experience: 1+ year in Proposal Development, Pricing, Budgeting, or related field About the Role IQVIA is seeking a Proposal Developer to join our Central Labs team. In

As a member of IQVIA’s Identity and Access Management (IAM) team, the Senior Business Analyst will be responsible for gathering, analyzing, and managing requirements that support the delivery of IQVIA’s enterprise information security solutions and capabilities. This role plays a critical part in en

IQVIA™ – The Human Data Science Company™ – is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences and healthcare industries. Our mission is to create intelligent connections that deliver unique innovations and actionable insights

Join a Team That’s Advancing Clinical Research We’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studi

Job OverviewApply knowledge and expertise including complex decision-making activities to review, assess and process Safety data and information across service lines. Recognized as specialist in one or more areas. Provide oversight on small to medium service operational projects and act as mentor to

Contract & Budget Sr Specialist. Develop the regional contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Essential Functions Coordinate the development of

Junior Site Activation Coordinator Location: Serbia or Bulgaria (Home-Based)Employment Type: Full-Time Job Overview We are seeking a motivated and detail-oriented Junior Site Activation Coordinator to join our team. In this Home-based role, you will support and coordinate site activation activities

To be eligible for this position, you must reside in the same country where the job is located.Job Overview Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Essential

Principais Responsabilidades: Participar da análise e do entendimento do escopo dos projetos demandados pelo PMO. Atuar no desenvolvimento, customização e replicação das soluções existentes da IQVIA. Apoiar o gerenciamento da fila de Suporte Nível II, atuando na resolução de issues e em demandas ad

Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Developing professional individual contributor who works under moderate

🚀 Lead Global Clinical Trials That Change Lives 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. CTM II

IQVIA Biotech collabore exclusivement avec des entreprises de biotechnologie et des sociétés biopharmaceutiques émergentes pour soutenir le développement clinique à toutes les phases et dans tous les domaines thérapeutiques. Notre structure agile, notre culture collaborative et notre expertise théra

Job Overview This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of t

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, init

Job OverviewThis individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, the ability to adapt quickly to chang

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, in

Job OverviewIndependently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide hig

Job Overview Manage and support team of Data Management professionals to efficiently produce databases that meet customer requirements. Essential Functions • Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF, database design and set-up, validation

Job Responsibilities: Complete maintenance of reference data (healthcare Organizations and Prescribers) as essential for UK Production. Perform research such as Internet Search, Phone Verification, Database Matches and etc. to gather information from third parties that will validate the completeness