Jobs at IQVIA

Drafts, revises, and negotiates study contracts, budgets, and scopes of work. Collaborates with project management, operations, and finance to update budgets in Excel. Leads negotiations for assigned agreements, tracks outstanding issues, mentors peers, supports process improvements, and serves as primary customer interface for medium-complex contracts.

Performs country-level clinical trial site activation and start-up activities for UK studies. Serves as a key contact for investigative sites and project teams, prepares and quality-checks regulatory and contractual documents, tracks approvals and timelines, maintains clinical systems and databases, monitors site performance, and provides UK regulatory and clinical trial expertise. Ensures compliance with applicable regulations, SOPs, work instructions, and project requirements.

Creates digital and print visual assets, presentations, infographics, web graphics, iconography, and basic multimedia content for global business units. Translates business requirements and creative direction into brand-compliant designs using Adobe Creative Cloud and PowerPoint. Collaborates with stakeholders, incorporates feedback, manages multiple deadlines, supports creative concept development, and performs basic video editing, animation, motion graphics, and photo retouching.

Serve as the senior data coordinator for complex clinical studies, leading data management tasks and acting as the primary project contact. Ensure data quality, resolve data clarification forms, support study start-up through close-out, coordinate timelines and sponsor communications, prepare data transfers, maintain study records, support audits, mentor team members, and assist with database and technology revisions.

Leads clinical data management operations across global clinical trials and central laboratory studies from startup through database lock. Oversees teams, timelines, budgets, quality, resources, customer negotiations, and project delivery. Provides technical expertise, process improvement, mentoring, quality control, SOP development, and technology implementation. Requires substantial experience managing multiple complex studies, large patient populations, and customer-facing negotiations.

Supports clinical trial delivery by maintaining study documents and systems, coordinating clinical supplies, tracking case report forms and queries, reviewing study files, and supporting CRAs and regulatory teams. Serves as a communication contact, mentors junior CTAs, assists with onboarding and interviews, may support site visits, and contributes to quality and process improvement initiatives.

Conducts clinical trial site monitoring and management across selection, initiation, monitoring, and close-out visits. Ensures protocol, GCP, ICH, regulatory, and sponsor compliance; supports recruitment, training, regulatory submissions, documentation, data queries, and study progress tracking. Maintains TMF and ISF records, prepares monitoring reports and action plans, collaborates with study teams, and may support site financial management and recruitment planning.

Design, build, and operate scalable backend systems, APIs, and data pipelines for ingestion, processing, validation, reconciliation, and reporting. The role includes developing reliable and observable systems, implementing CI/CD and monitoring, using AI-assisted development tools, supporting cloud and containerized environments, and mentoring engineers. The developer will own solutions end to end and collaborate with product, analytics, and data teams.

Perform site selection, initiation, monitoring and close-out visits per GCP/ICH for interventional studies. Manage recruitment plans, regulatory submissions, TMF/ISF documentation, CRF completion, data queries, and site communications. Escalate quality issues and collaborate with study teams.

Conducts quality assurance testing for complex software applications supporting client implementation projects. Develops test plans and cases, executes manual and automated tests, tracks defects, reports results, and coordinates troubleshooting with developers, business analysts, technical leads, consultants, and other stakeholders throughout the SDLC. Documents risks, escalates issues, and identifies opportunities for expanded test automation.

Provides clinical data management support for clinical studies, serving as a Data Operations Coordinator or task lead under supervision. Responsibilities include data review, clarification resolution, database development and testing, audit leadership, programming testing, clinical data coding, and compliance with operating procedures. The role requires collaboration with CDM teams, strong organization and communication, attention to detail, initiative, and leadership capabilities.

Leads statistical activities for real-world evidence and clinical research studies, including protocol review, SAP development, methodology, analysis oversight, deliverable review, results interpretation, client interactions, proposals, and staff mentoring. Ensures compliant, timely, high-quality statistical reporting and supports cross-functional teams.

Manages the creation and quality assurance of global pharmaceutical data elements. Conducts in-depth research and analysis for data standards, complex projects, and client queries. Leads teams, schedules daily data activities, recommends process improvements, contributes to system development, and manages global data standards and quality assurance initiatives.

Oversee financial and contractual operations for global clinical service projects, including revenue recognition, forecasting, invoicing, backlog management, variance analysis, contract compliance, and customer reporting. Partner with finance, legal, pricing, and operational teams to address financial issues, improve processes, support business reviews, and ensure accurate, timely deliverables. Provide training and guidance to operational teams while serving as a key customer contact.

Develops, tests, validates, and documents SAS programs for statistical tables, figures, listings, analysis databases, data transfers, and quality control checks. Integrates data from multiple studies, develops macros and applications, leads statistical programming activities for studies, manages scope and resource requirements, and mentors junior staff. Requires collaboration with internal and external clients and expertise in clinical drug development and statistical programming.

Leads a portfolio of decentralized clinical trial projects, coordinating sponsors, sites, clinicians, and cross-functional teams. Oversees budgets, forecasting, documentation, metrics, quality risks, corrective actions, change control, training, and milestone delivery. Builds and mentors project teams while ensuring compliance with clinical research regulations, protocols, and applicable laws.

Supports patient-centered research, HEOR, PRO, clinical outcomes, and evidence-generation projects for pharmaceutical, biotechnology, and healthcare clients. Conducts qualitative and quantitative research, analyzes healthcare evidence, develops reports and presentations, assists with proposals, manages stakeholders, and supports client meetings. The role is fully remote in Mexico and requires experience in outcomes research, patient-reported outcomes, real-world evidence, epidemiology, or related healthcare research.

Lead and manage consulting engagements for pharmaceutical and life sciences clients across North LATAM. Serve as primary client contact, oversee project timelines, budgets, deliverables, and quality. Conduct market research and present recommendations, mentor junior consultants, and support business development and account growth.

Supports the Labmatrix Product team by facilitating Agile ceremonies, translating business needs into user stories and requirements, managing backlog documentation, tracking Agile metrics, streamlining workflows with emerging technologies, and coordinating user acceptance testing and defect tracking.

Supports solution implementations by coordinating milestones, gathering requirements, creating and executing test cases, maintaining validation quality, and developing documentation and training materials. Collaborates with customers, engineering, product development, and project management teams to improve platform functionality, integrations, implementation practices, and production support processes.