IQVIA

Analyst

• Develop materials and services for UK HTA and HEOR project delivery, including dossier writing, early HTA scientific advice, HTA landscape reviews, literature reviews, health economic model development and adaptations, submission support, and pricing negotiation support
• Contribute to multi-country HTA and HEOR projects across different markets and product types
• Develop strategic HTA knowledge and skills, especially UK HTA processes and requirements
• Collaborate with internal project teams, client teams, technical consultants, Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies, and local teams globally
• Support thought leadership through conference abstracts and posters, HTA white papers, and guidance of interns working on HTA-focused thesis topics
• Develop knowledge of global HTA and HEOR offerings to support business development
• Work flexibly across multiple projects and complete assigned tasks within core company working hours and deadlines
• Participate in training and receive development support through the buddy system and regular 1:1 meetings

Analyst, UK Health Technology Assessment Strategy and Implementation

Consultant

• Shape and lead the team and offerings with senior leadership and global centres of excellence
• Manage business development and client relationships, including understanding strategic goals and milestones
• Confirm, manage, and maintain project scope to meet client goals efficiently
• Manage HTA project strategy and direction, particularly UK HTA processes and requirements
• Identify potential challenges to product value and develop risk mitigation strategies
• Manage project delivery teams on dossier development, UK HTA submission support, early scientific advice, HTA strategy, and strategic HTA offerings
• Contribute to multi-country and global HTA projects
• Mediate, negotiate, and solve problems within and outside project teams
• Train and identify opportunities for junior team members' career development
• Collaborate across IQVIA teams, including technical consultants and Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies, and local global-network teams
• Liaise with pharmaceutical, biotechnology, and medical device clients and affiliate teams
• Support or lead HTA thought leadership, including conference abstracts, posters, white papers, and peer-reviewed publications
• Guide interns working on HTA-focused thesis topics
• Provide line management, depending on interests

Senior Consultant – HTA, UK Market

• Develop materials and services for UK HTA and HEOR project delivery, including dossier writing, early HTA scientific advice, HTA landscape reviews, literature reviews, health economic model development and adaptations, submission support, and pricing negotiation support
• Contribute to multi-country HTA and HEOR projects across different markets and product types
• Develop strategic HTA knowledge and skills, particularly in UK HTA processes and requirements
• Collaborate with internal project teams, client teams, technical consultants, Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies, and local teams across IQVIA’s global network
• Support HTA thought leadership through conference abstracts, posters, white papers, and guidance of interns on HTA-focused thesis topics
• Develop knowledge of global HTA and HEOR offerings to support business development opportunities
• Work flexibly across multiple projects and complete assigned tasks within core company working hours and deadlines

Analyst, Health Technology Assessment Strategy and Implementation

Learning and Development

• Develop Sales Professionals learning and coaching activities that increase performance and business results across the nation
• Enhance selling skills, product knowledge, account management capability, and territory business acumen
• Partner with Managers and work with specific districts to improve selling skills and sales model competencies
• Apply adult learning principles, facilitation skills, and innovative learning solutions to execute training programs
• Conduct field rides, virtual coaching sessions, and live classroom training
• Conduct environmental scans across the Region and Nation to identify learning gaps
• Maintain current healthcare environment, marketplace, product, and selling skills expertise
• Deliver training deliverables on-time and on-budget
• Develop, obtain approval for, and deliver disease state, treatment, product, marketplace, foundational, and advanced sales skills training
• Consult with Sales Leadership to identify training needs and gaps
• Keep current on trends in training, performance improvement, and organizational learning
• Maintain and build contacts with training vendors and training professionals
• Monitor course evaluations and compliance metrics for continuous improvement
• Facilitate meetings and training sessions using effective platform skills
• Travel in the field to coach individual sales representatives
• Demonstrate selling skills regarding the client’s portfolio to meet customer needs
• Continually develop and apply adult learning principles and new learning techniques

Training Manager

Sales

• Oversee operations of IQVIA Field Coordinators and Pharmaceutical Sales Representatives promoting approved client products to healthcare professionals
• Deliver contractual obligations and personnel and administrative requirements
• Serve as the client’s main point of contact regarding commercial project work
• Create, manage, and maintain project plans, timelines, milestones, business rules, and workflows
• Facilitate communication with internal and external stakeholders through status reports and project meetings
• Monitor and report performance, progress, KPIs, scorecards, priorities, and key deliverables
• Provide updates and feedback to internal and client stakeholders
• Apply operational knowledge throughout the project lifecycle
• Identify trends and obstacles to achieving project goals
• Manage cross-functional collaboration to achieve operational deliverables and milestones
• Conduct personnel and HR actions including hiring, performance management, development or disciplinary plans, terminations, and personnel issue resolution
• Support and oversee HR actions conducted by first-line managers for Sales Representatives
• Review and approve first-line manager expense reports and monitor expense-policy compliance
• Coordinate meetings and associated components as needed

Project Lead – National Sales

Project Manager

• Support the development and execution of go-to-market collateral in partnership with Creative and Execution teams
• Assist Product Managers with campaign planning, coordination, and scheduling
• Manage multiple campaigns simultaneously in a high-volume environment
• Review and edit content produced by writers and copy editors to ensure quality and accuracy
• Ensure a high standard of written English across campaign and product-related materials
• Collaborate with cross-functional stakeholders to support campaign execution and delivery
• Prioritize competing activities and deadlines while maintaining attention to detail
• Communicate effectively with stakeholders to ensure alignment and progress across projects

Commercial Services Project Manager

Associate

• Support the development and execution of go-to-market collateral in partnership with Creative and Execution teams
• Assist Product Managers with campaign planning, coordination, and scheduling
• Track and coordinate multiple campaigns and deliverables simultaneously
• Review and edit content produced by writers and copy editors to ensure quality and consistency
• Ensure a high standard of written English across campaign and product-related materials
• Coordinate with cross-functional stakeholders to support campaign execution and delivery
• Maintain project timelines, track progress, and communicate updates to stakeholders
• Manage competing priorities while maintaining attention to detail

Associate, Commercial Services

Medical writer

• Acts as Lead Medical Writer on most types of writing projects
• Prepares assigned documents according to IQVIA SOPs, customer requirements, and agreed timelines
• Performs Senior Review of straightforward medical writing deliverables
• Negotiates timelines and discusses/resolves customer comments
• Provides written and verbal feedback to junior staff and customers when appropriate
• Keeps current with medical, technical writing, regulatory knowledge, and GCP developments
• Leads preparation of assigned documents, confirms scope, templates, specifications, timelines, reviews, and customer communication
• Plans and organizes workload, tracks timelines, and implements customer requests
• Leads meetings on challenging topics
• Presents Medical Writing processes at bid defense meetings
• Assists with training and development of junior staff and may deliver global team training
• May act as Project Manager for complex Medical Writing projects, including finance and invoicing responsibilities
• Completes project finance activities, including monitoring and forecasting budgeted hours
• Proposes, reviews, and approves routine project budgets and costings
• May take on customer lead responsibilities or assist partnership leads
• May represent the region or site on Medical Writing and cross-functional initiatives
• Facilitates identification of new ideas and may represent Medical Writing at capabilities audits

Principal Medical Writer

Software Engineer

• Review submission-ready ADaM datasets, tables, figures, listings and submission packages
• Provide expertise in designing, developing and quality-controlling SAS programs for accessing, extracting, transforming, reviewing, analyzing and submitting clinical data
• Collaborate with study teams on data structures and specifications for ADaM datasets, tables, figures, listings and analysis submission content
• Ensure clinical data quality, accuracy and submission readiness according to regulatory requirements, including SDTM, ADaM, tables, figures, listings and define.xml
• Lead pooled and exploratory analyses with Statistics TA leads, study statisticians and clinical programming teams
• Lead in-house specification and delivery of ISS and ISE datasets and associated outputs when not provided by CROs
• Lead design and implementation of complex SAS programs for analyzing and reporting clinical trial data in CDISC ADaM format
• Lead development of global tools to increase Statistical Programming group efficiency and capacity
• Plan and execute activities with clinical study teams to meet project timelines and deliver high-quality outputs
• Collaborate with CR&D staff on data analysis requests
• Perform additional statistical analyses supporting regulatory responses, integrated safety and efficacy summaries, publications, presentations, and clinical trial planning and reporting

Senior Statistical Programmer – FSP

Nurse

• Assess and monitor patient therapy under physician direction and supervision
• Assist physicians with examinations and procedures
• Maintain efficient and appropriate patient flow
• Perform venipuncture, access implanted ports, and maintain central venous access devices and alternate delivery systems
• Document all elements of patient care
• Communicate pertinent information and interventions to physicians or mid-level providers
• Serve as a resource to medical assistants and LPNs
• Triage patient/family phone calls and document relevant information
• Assess patient/family needs and provide teaching
• Assist with referrals using community resources when necessary
• Mentor/precept and provide day-to-day guidance to less experienced nurses
• Confirm informed consent before study-specific tasks
• Identify patients requiring increased nursing assessment and collaborate with the healthcare team to ensure safety
• Educate patients regarding study procedures and protocol-agent adherence
• Collaborate with investigators on treatment schedules and drug-dose modifications
• Coordinate communication between research and clinical staff
• Provide evidence-based symptom management as permitted by protocol
• Administer investigational compounds and/or chemotherapy/biotherapy according to protocol and regulations
• Perform protocol-required labs, samples, vital signs, and ECGs
• Record study procedures, medication lists, and infusion reactions

Infusion Nurse

• Manage the operational delivery of Interactive Response Technology (IRT) projects and programs
• Work with clients to understand study protocols and translate requirements into effective IRT solutions
• Manage projects throughout the delivery lifecycle
• Coordinate cross-functional teams, timelines, budgets, invoices, risks and milestones
• Author User Requirements Documents (URDs) and review requirements with clients and internal stakeholders
• Support the design, build and implementation of study systems
• Ensure delivery aligns with the Sponsor's study protocol, agreed requirements, quality standards and timelines
• Lead problem-solving and issue-resolution activities
• Perform internal User Acceptance Testing (UAT) following study validation
• Manage and support client UAT activities and clarify study or system requirements
• Coordinate resolution of testing issues
• Identify and implement process improvements with other Project Managers
• Contribute to project proposals and Requests for Proposal (RFPs)
• Participate in proposal development and sales or client presentations
• Ensure compliance with established processes, policies, procedures and project standards

Project Manager – IRT System Design

Manager

• Provide strategic oversight and project management for global or multi-regional Site Activation activities
• Lead start-up delivery from pre-award through activation and lifecycle maintenance in compliance with ICH-GCP, regulatory requirements, and project timelines
• Develop and execute the Site Activation Management Plan aligned with study strategy and scope of work
• Collaborate with internal teams, regions, and external stakeholders to ensure efficient study start-up execution
• Oversee regulatory submissions, approvals, contracts, and essential document processes
• Assess regulatory landscapes and contribute to regulatory intelligence and strategy
• Identify risks and propose practical solutions to support study delivery and bid processes
• Ensure accurate tracking, reporting, and maintenance of project systems, timelines, and documentation
• Support business development, including bid defense and client engagement activities
• Mentor and coach team members and contribute to continuous improvement initiatives
• Build and maintain strong client relationships and support customer-facing activities

Global Site Activation Manager

Clinical Trial Assistant

• Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems, including the Trial Master File (TMF), that track site compliance and performance within project timelines.
• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
• Assist with periodic review of study files for completeness.
• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

Site Activation Manager – Sponsor Facing

QA Engineer

• Plan, schedule, conduct, report and close audit activities in countries involved with IQVIA contracts
• Assess compliance with regulations, guidelines, customer requirements, IQVIA SOPs, and project-specific guidelines/instructions
• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers
• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, policies, and procedures
• Consult customers and monitors on audit observations and corrective action plans
• Review and approve investigations, Root Cause Analysis, CAPA, and Effectiveness Check plans, and track them to closure
• Evaluate policies and procedures and recommend continuous process improvements
• Maintain the electronic quality management system and support the audit lifecycle
• Lead, collaborate on, and support quality assurance initiatives and process improvement projects
• Assist in training new Quality Assurance staff
• Manage Quality Issues as required
• Present educational programs and guide operational staff on compliance procedures as required
• Perform pre-inspection visits, host audits/inspections, ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections as assigned