IQVIA

Field Engineer

• Perform hydraulic assembly removal and replacement on fielded dialysis machines in accordance with approved work instructions and customer requirements.
• Complete system rinse, flush, testing, and calibration activities required after hydraulic assembly replacement.
• Accurately document service completion, unit status, results, exceptions, and follow-up needs in designated tracking systems or customer workflows.
• Coordinate with field leadership, schedulers, program management, and customer site contacts to support efficient routing and timely completion of assigned work.
• Follow all applicable safety, quality, documentation, and compliance expectations while working in active clinical environments.
• Support logistics coordination related to receipt, movement, staging, and return or disposition of hydraulic assemblies and related materials.
• Communicate schedule risks, access issues, incomplete site data, product concerns, or service barriers promptly to field leadership and program management.
• Provide updates, reports, and field-level feedback to support documentation, completion tracking, and continuous improvement throughout the program.
• Maintain professional conduct when interacting with customer personnel, clinic staff, and internal IQVIA/client stakeholders.
• Support after-hours and weekend coverage as needed based on clinic availability, site access windows, and program timelines.

MedTech Field Service Engineer, Dialysis, Hydraulics

Data Analyst

• Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams.
• Perform, manage and co-ordinate activities for assigned opportunities/projects.
• Perform data mining and analysis, formulate recommendations and present to internal and potentially external stakeholders.
• Accountable to ensure IQVIA planning services are providing a competitive edge in winning new business.
• Make recommendations for IQVIA commitments of future studies by delivering accurate and robust country, site or enrollment strategies in support of opportunities including but not limited to requests for proposals, early engagements, re-bids and potentially awarded studies.
• Support the development of materials related to feasibility or site lists or enrollment strategies for customer bid defense meetings or internal customers such as Therapeutic Strategy Leads, Medical Leads or business development.
• Collaborate with key stakeholders and IQVIA project teams to resolve issues.
• Prepare for planning meetings by conducting research into therapeutic areas using databases, scientific literature, the internet and expert medical knowledge.
• Be involved in planning meetings with internal stakeholders including Medical Directors, Therapeutic Strategy Leads, Business Developers, Sales Staff and Program Directors. Present results of data gathering and analysis activities.
• Undertake therapeutic training, as necessary, and keep abreast of developments in clinical research.
• Proficient with planning tools, demonstrate a good understanding of system features and functions to know what features are best used to accomplish an accurate country, site or enrollment strategy.

Global Analytics Specialist

General

• Conduct outreach and training for investigator sites opting into RRC services
• Train and onboard research clinicians, ensuring they are prepared and study-ready
• Manage access to systems like Study Hub and Thinking Cap for both site staff and clinicians
• Receive and process Visit Request Forms (VRFs)
• Assign and confirm clinicians for remote visits
• Coordinate visit logistics including supplies, equipment, and courier services
• Ensure all required documentation (e.g., DOA logs, clinician credentials) is complete and uploaded
• Maintain and update Smartsheet trackers for sites, visits, and clinicians
• Perform quality checks on source documents and ensure timely corrections
• Review uploaded documents in Study Hub and notify relevant stakeholders
• Deliver study-specific training to sites and clinicians
• Ensure compliance with GCP, ICH, HIPAA, and IQVIA SOPs
• Serve as the primary liaison between sites, clinicians, and internal study teams
• Provide ongoing support and retraining to clinicians and sites as needed
• Escalate issues to RRC Lead and ensure resolution

Visit Coordinator, US Regional Specialist

Consultant

• Contribute to the development of German AMNOG dossiers, with a focus on Modules 2–4
• Perform scientific assessment of clinical trial data, including efficacy, safety, patient-relevant endpoints, and subgroup analyses
• Conduct systematic literature reviews and structured evidence syntheses
• Medical writing, including: AMNOG dossier texts and updates
• Written statements and responses for G BA procedures and hearings
• Scientific reports, slide decks, and selected publications
• Support indirect treatment comparisons and interpretation of statistical outputs
• Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)
• Ensure scientific quality, clarity, and consistency of HTA-related documents
• Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies

Health Technology Assessment Consultant, German

Clinical Research

• Contribute to the development of German AMNOG dossiers
• Perform scientific assessment and analysis of clinical trial data
• Perform meta-analyses and indirect treatment comparisons
• Contribute to the automation and standardization of analysis workflows
• Ensure scientific quality, clarity, and consistency of generated outcomes

Biostatistician, SAS, R – German HTA submissions

• Lead day-to-day activities of multiple evidence synthesis projects with the support of junior team members
• Provide senior technical and statistical leadership and effective ad hoc problem-solving support
• Edit, review, and develop scripts to ensure accurate and efficient implementation
• Support project implementation including overall project management and client engagement
• Conceptualize evidence synthesis engagements in response to client request for proposals
• Mentor and coach junior statisticians and project delivery teams

Senior Consultant – Evidence Synthesis, Global Health Economics

• Lead day-to-day activities of multiple evidence synthesis projects with the support of junior team members
• Provide senior technical and statistical leadership and effective ad hoc problem-solving support to the delivery of diverse evidence synthesis projects
• Full proficiency and demonstrable coding/programming experience in WinBUGS, OpenBUGS, JAGS and R is required, and knowledge of Stan is desirable
• Support project implementation including overall project management and client engagement
• Conceptualize evidence synthesis engagements in response to client request for proposals
• Drive the development of innovative methods and the dissemination of research outputs in peer-reviewed journals and scientific conferences
• Serve as a line manager for junior staff members

Clinical Operations

• Leading global cross-functional project team delivery
• Serving as the primary contact with the customer for progress and governance
• Developing study management plans
• Anticipating risk and implementing mitigation strategies
• Managing study budget proactively

Clinical Program Manager

Data Scientist

• Lead data management for complex, global clinical trials from study setup to database lock
• Serve as the main client contact for all data management deliverables
• Oversee SAE, PK, and external data reconciliation and database deployment
• Manage timelines, budgets, and resource allocation to meet customer expectations
• Mentor junior data management staff and promote best practices
• Drive process improvements and ensure regulatory and SOP compliance

Senior Data Management Lead

Analyst

• Participates in the design, development, and delivery of solutions for clients
• Reviews and analyzes client requirements or issues
• Provides guidance and advice to others within IQVIA
• Prepares documentation and detailed specifications
• Follows up with clients to ensure their satisfaction

Technology Analyst

• Participe dans la conception, le développement et la livraison de solutions pour les clients
• Passe en revue et analyse les exigences ou les enjeux des clients
• Élaborer une documentation et des spécifications détaillées
• Conçoit, structure et fournit des rapports et des présentations clients adaptés
• Assure un suivi avec le client une fois les livrables du projet terminés

Analyste en technologies – Technology Analyst

Reviewer

• Producing materials and services relating to Health Economics Outcomes Research business areas
• Involved in shaping and leading the team and offerings
• Independently develop searches in various databases and proficient in using OVID SP or similar platforms
• Keeps up to date on new methodologies and HTAs requirements for systematic literature reviews
• Manage literature review projects with senior oversight
• Guides the team on interpretation/qualitative synthesis of the literature review findings
• Conducts quality control of literature review deliverables
• Oversees the development of research questions, PICOS criteria, search strategies and literature review protocols
• Collaborates with other business areas to deliver client services

Literature Reviewer

Strategy

• Lead the development of delivery strategies for large, complex, multi-region clinical studies (including mega studies)
• Partner with Sales, Medical, and Operations teams to win new business and achieve revenue targets
• Translate client needs into effective, competitive, and feasible clinical trial strategies
• Evaluate feasibility, risks, country/site selection, and patient recruitment strategies
• Develop and review project budgets aligned with pricing strategy and margin targets
• Support proposal development, client presentations, and bid defense meetings
• Ensure seamless handover of strategy to project delivery teams
• Monitor study progress and adjust strategies as needed
• Contribute to long-term business growth through cross-functional collaboration

Associate Therapeutic Strategy Director

Inside Sales

• Work closely with Johnson and Johnson client partners resource teams
• Utilize a multifaceted approach to communicate with key accounts
• Conduct outbound calls to enhance product knowledge
• Educate via Zoom or live face to face with key stakeholders
• Serve as the key conduit for resource allocation and utilization within the territory
• Convey complex clinical, diagnostics and access information to customers

Oncology Inside & Field Sales Specialist – Southeast/South Central

• Provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers
• Provide in-service presentations with the goal to increase patient enrollment
• Work in partnership with CRAs and other field-based medical teams for optimal trial execution, developing tailored recruitment plans
• Develop referral networks to support the sites, as well as work with support groups in the therapeutic area

MedTech Field Service Engineer, Dialysis, Hydraulics

Global Analytics Specialist

Visit Coordinator, US Regional Specialist

Health Technology Assessment Consultant, German

Biostatistician, SAS, R – German HTA submissions

Senior Consultant – Evidence Synthesis, Global Health Economics

Senior Consultant – Evidence Synthesis, Global Health Economics

Clinical Program Manager

Senior Data Management Lead

Technology Analyst

Analyste en technologies – Technology Analyst

Literature Reviewer

Associate Therapeutic Strategy Director

Oncology Inside & Field Sales Specialist – Southeast/South Central

Site Enrollment and Engagement Lead – Registered Nurse