IQVIA

Scientist

• Define and execute a forward-looking scientific strategy aligned to evolving client and industry needs
• Drive adoption of AI-assisted design, predictive modelling, automation, computational sciences, and translational approaches
• Provide scientific leadership across a diverse discovery portfolio, ensuring excellence, rigour, and translational relevance
• Support strategic client engagements, proposals, partnerships, and business growth opportunities
• Act as a senior scientific ambassador with clients, collaborators, and industry stakeholders
• Mentor and inspire multidisciplinary teams across biology, chemistry, protein design, pharmacology, translational, and computational sciences

Chief Scientist – Modern Drug Discovery

Field Engineer

• Install hardware for automated medication dispensing systems within healthcare facilities throughout the United States
• Organize, test, and assemble automated medication dispensing systems
• Install and configure hardware, software, and mechanical medical devices
• Review schematics, drawings, documentation, and logistics to support installation activities
• Conduct routine checks and record data from product tests after installation and configuration
• Ensure work is completed in accordance with quality compliance requirements
• Partner with support staff and manage project timelines and customer needs
• Travel 100% locally, regionally, and nationally
• Work assignment-based schedules typically involving 16–30 hours per week plus travel time
• Enter healthcare facilities and complete facility credentialing processes

MedTech Device Field Service Engineer, Technician

Software Engineer

• Program, test, and document statistical tables, figures, listing summaries, analysis databases, derived datasets, and data transfers
• Program integration of databases from multiple studies or sources
• Develop programming documentation, plans, and specifications
• Provide advanced technical expertise and project solutions to internal and external clients and teams
• Develop, implement, and validate process technologies, macros, and applications
• Fulfill statistical team lead responsibilities for single studies under supervision
• Understand scopes of work, estimate completed work, and manage out-of-scope work for single studies
• May manage budgets and resource requirements and provide revenue and resource forecasts
• Provide training and guidance to lower-level and new staff

Stat Programmer II

User Researcher

• Lead UX research and design activities throughout the product lifecycle, including discovery, problem framing, research planning, synthesis, ideation, prototyping, validation, delivery, and continuous improvement
• Plan and conduct qualitative and quantitative research to understand user needs, behaviors, workflows, pain points, and decision-making contexts
• Translate research findings into actionable insights, product recommendations, design direction, and requirements
• Design and evaluate user experiences for AI-enabled products, including LLM-based applications, agentic systems, intelligent automation workflows, and human-in-the-loop decision-support solutions
• Create and maintain UX artifacts, including personas, journey maps, service blueprints, workflow models, wireframes, prototypes, usability reports, and design specifications
• Collaborate with product managers, engineers, data scientists, clinicians, and business stakeholders
• Contribute to rapid experimentation, iterative delivery, measurement, and continuous learning within small agile teams
• Provide leadership in ambiguous environments and influence product direction through data- and research-driven insights
• Mentor UX professionals and cross-functional team members
• Advocate for accessibility, usability, ethical AI principles, and human-centered design

Senior UX Researcher, Designer

• Install hardware for automated medication dispensing systems within healthcare facilities
• Organize, test, and assemble automated medication dispensing systems
• Install and configure hardware, software, and mechanical medical devices
• Review schematics/drawings, documentation, and logistics to support installation activities
• Conduct routine checks and record data from product tests after installation and configuration
• Ensure work is completed in accordance with quality compliance requirements
• Partner with support staff, manage project timelines, and address customer needs
• Travel 100% locally, regionally, and nationally
• Work assignment-based schedules, typically 16–30 hours per week plus travel time
• Collaborate with healthcare professionals and lead technical initiatives in medical device technology

MedTech Device Field Service Engineer

Project Manager

• Participate in bid defense presentations with Business Development
• Lead presentations for smaller, less complex regional studies when applicable
• Deliver and manage smaller, less complex regional studies when applicable
• Develop integrated study management plans with the core project team
• Execute clinical studies according to contracts, SOPs, policies, and procedures while optimizing speed, quality, and cost
• Set objectives for core project teams and sub-teams; communicate and assess performance
• Collaborate with internal functional groups to achieve milestones and manage study issues
• Monitor progress against contracts and present project information to internal and external stakeholders
• Proactively manage risks, contingencies, problem solving, and resolution efforts
• Identify quality risks and implement corrective and preventative action plans
• Serve as primary or backup customer contact and manage key customer relationships
• Build and lead cross-functional project teams and oversee overall project delivery
• Ensure project financial success and identify opportunities to accelerate revenue
• Identify scope changes and manage the change control process
• Identify lessons learned and implement best practices
• Lead vendor management activities when assigned
• Support corporate initiatives and act as a change advocate
• Provide input on project team members' performance
• Mentor less experienced project team members and support their professional development

Project Manager, Study Operations

Clinical Operations

• Direct a team of clinical staff supporting clinical studies to ensure appropriate resourcing, training, and achievement of project objectives
• Work with senior leadership to formulate strategic goals and objectives and ensure operational alignment with organizational priorities
• Manage staff, including planning, assigning, and directing work; appraising performance; guiding professional development; rewarding and disciplining employees; and resolving employee relations issues
• Direct hiring and selection for clinical staff and ensure new employees are onboarded and trained
• Ensure staff have materials, systems access, and training; oversee training plans, SOP review, and training experiences
• Allocate resources to clinical research projects by assigning appropriately trained staff
• Manage the quality of assigned staff's clinical work through regular review and evaluation of work products
• Identify quality risks and issues and create corrective action plans
• Monitor workload, quality, and budget metrics through regular review and reporting
• Collaborate with regional and/or global clinical, client, and functional leadership teams to manage project challenges and deliver exemplary customer service
• Participate in corporate or organizational quality and process improvement initiatives
• Act as a client liaison in day-to-day relationship governance, escalations, and client-facing initiatives
• May manage other managers

Associate Director, Clinical Operations

• Install hardware for automated medication dispensing systems within healthcare facilities
• Organize, test, and assemble automated medication dispensing systems
• Install and configure hardware, software, and mechanical medical devices
• Review schematics, drawings, documentation, and logistics to support installation activities
• Conduct routine checks and record data from product tests after installation and configuration
• Ensure work is completed in accordance with quality compliance requirements
• Partner with support staff and manage project timelines and customer needs
• Travel 100% locally, regionally, and nationally
• Work assignment-based schedules, typically 16–30 hours per week plus travel time
• Collaborate with healthcare professionals and lead technical initiatives in medical device technology

• Establish and manage performance dashboards; analyze event triggers and alerts and determine appropriate follow-up
• Manage project schedules and update key milestones
• Coordinate and lead risk and issue management processes
• Manage project finances, including EAC, monthly expenses, invoices, and reconciliation
• Identify out-of-scope activities and maintain change-control processes
• Manage vendor plans and purchase-order processes; assess vendor risks
• Provide project data on cost, schedule, scope, utilization, change orders, and quality
• Develop and maintain sections of Project Management Plans and support project-management system improvements
• Review project resource allocation within budget
• Prepare correspondence, meeting minutes, status reports, and presentation materials
• Organize internal project-team and customer meetings with the Project Leader
• Lead core study file reviews, support audits, and drive eTMF filing compliance
• Manage project-specific eTraining and oversee team compliance
• Coordinate onboarding and system access for key project team members
• Monitor project metrics and update IQVIA systems for accurate reporting
• Participate in regional and global PMA initiatives
• Mentor less experienced Project Management Analysts

Senior Project Management Analyst

• Develop process methodology for the department to meet internal and external clients’ needs
• Plan and coordinate integrated programming solutions across statistical programming needs
• Provide technical expertise and leadership to the department
• Provide internal consulting services, including specifications and user needs analysis for complex projects or client requirements
• Program, test, and document statistical programs for tables, figures, and listing summaries
• Program analysis databases and data transfers for internal and external clients
• Plan programming of database quality control checks
• Integrate databases from multiple studies or sources
• Develop and coordinate programming documentation, plans, and specifications
• Provide advanced technical expertise and project solutions for complex studies
• Develop, implement, and validate process technologies, macros, and applications
• Fulfill statistical team lead responsibilities for complex studies
• Understand scope of work, budgets, and quote assumptions; estimate work completed; manage out-of-scope work and resource forecasts
• Provide training and guidance to lower-level staff

Senior Statistical Programmer

Document Specialist

• Coordinate the development, compilation, review, and finalization of Clinical Study Report appendices
• Lead CSR appendices kickoff meetings and define timelines with the CSR sub-team
• Format CSR appendices according to templates, style guides, and regulatory requirements
• Develop the Financial Disclosure and BIMO module for submission studies as required
• Maintain version control throughout the document lifecycle
• Perform quality control checks on CSR appendices
• Ensure compliance with SOPs, ICH guidelines, and submission standards
• Support document review workflows, approval processes, and submission-ready publishing
• Coordinate document development, review, and approval timelines
• Monitor project milestones and escalate delivery risks
• Support inspection and audit readiness activities
• Maintain document repositories and archival records in electronic document management systems
• Follow data integrity and confidentiality requirements
• Improve TMF document processes and contribute to process optimization initiatives

CSR Document Specialist

QA Automation Engineer

• Plan, deploy, document, and maintain new and existing network architectures, including SoNIC, Cumulus, and Cisco
• Support SDN solutions, focusing on Cisco ACI across multiple data centers
• Integrate AI-driven network monitoring and predictive analytics
• Serve as a senior technical advisor to Tier 2 engineers through mentorship and consultation
• Provide expert-level support during major incidents, including root cause analysis and resolution planning
• Translate Global Network Support standards into low-level designs, hardware quoting, and documentation
• Partner with M&A and Global Real Estate teams to integrate acquisitions into IQVIA network standards
• Lead network buildouts, office restack implementations, and refresh initiatives
• Lead strategic network projects across departments, regions, and time zones
• Automate F5 configurations, Palo Alto firewall rules, and Cisco ACI policies using Ansible, Python, Terraform, and/or APIs
• Implement CI/CD pipelines to validate and roll out network and security changes safely and repeatably
• Implement and support network segmentation strategies for zero-trust architectures and compliance mandates
• Oversee incident response and escalation workflows, ensuring timely resolution and stakeholder communication
• Maintain DNS (BIND), IPAM, and domain name services using automation-first principles
• Support branch office automation initiatives using Cisco DNA Center and other vendor platforms

Senior Network, Automation Engineer

Compliance

• Prepares and/or reviews regulatory submission documents supporting clinical trial and marketing authorization activities for internal and external clients.
• Provides regulatory support for assigned projects.
• Acts as a Regulatory Team Member on small, straightforward regulatory projects and/or participates in small single-service projects under senior guidance.
• Identifies project needs, tracks timelines, implements client requests, and manages day-to-day workload with senior staff.
• Prepares and/or reviews regulatory documentation within area of expertise.
• Participates independently in project teams with internal and external customers and communicates on straightforward matters.
• Understands project scope of work and deliverables.
• May prepare slides and background material for business development meetings and present in client meetings by phone or in person.
• May prepare and deliver trainings.
• Performs other tasks assigned by Regulatory management.
• Makes minor system and process changes to solve problems and improve effectiveness.

Regulatory Affairs Officer

Clinical Research

• Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits
• Adapt, drive, and track subject recruitment plans with study sites
• Administer protocol and study training to assigned sites
• Establish regular communication with sites to manage project expectations and issues
• Evaluate study-site practices for protocol quality, integrity, and regulatory adherence
• Escalate quality issues as appropriate
• Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution
• Support the study start-up phase when applicable
• Ensure site documents are available for Trial Master File filing
• Verify Investigator's Site File maintenance in accordance with GCP and local regulatory requirements
• Create and maintain site-management documentation, monitoring-visit findings, and action plans
• Submit visit reports and generate follow-up letters and other required study documentation
• Collaborate with study team members to support project execution
• Support development of project subject recruitment plans on a per-site basis when applicable
• Support site financial management and retrieve invoices according to local requirements when applicable

Clinical Research Associate – Sponsor Dedicated

Analyst

• Design and deliver upfront requirements to enable accurate downstream data for site payments across IQVIA proprietary systems
• Serve as a point of contact for IT groups and Payments groups, escalating to the System Alignment lead where necessary
• Deliver accurate site payment data for all IQVIA studies, regardless of whether IQVIA CTMS or DrugDev is used for payment
• Interpret EDC subject visit data, site contracts, payment system design and payment triggers
• Analyse data fallout and provide necessary corrections to ensure sites are paid accurately
• Resolve data flows on large, ongoing projects, escalating to the Data Alignment lead where necessary
• Interact with multiple internal IQVIA stakeholders
• Support the System Alignment lead in resolving EDC, Data Warehouse, CTMS or DrugDev system issues preventing payments

Chief Scientist – Modern Drug Discovery

MedTech Device Field Service Engineer, Technician

Stat Programmer II

Senior UX Researcher, Designer

MedTech Device Field Service Engineer

Project Manager, Study Operations

Associate Director, Clinical Operations

MedTech Device Field Service Engineer, Technician

Senior Project Management Analyst

Senior Statistical Programmer

CSR Document Specialist

Senior Network, Automation Engineer

Regulatory Affairs Officer

Clinical Research Associate – Sponsor Dedicated

Senior Data Services Analyst