IQVIA

Consultant

• Project management and delivery whilst maintaining high levels of client satisfaction
• Managing stakeholders in projects, including junior colleagues, seniors, and clients
• Reviewing and analysing client problems and assisting in the development of solutions and detailed documentation
• Performing quantitative and qualitative analyses
• Driving the design, structure, and completion of presentations to the client
• Developing and presenting client deliverables
• Proactively developing your knowledge of consulting methodologies and the life sciences market through deliverables and formal and informal learning opportunities
• Collaborating with colleagues on internal activities, such as recruitment, training, junior development, to continue supporting the growth and development of our team

Consultant – EMEA Life Sciences, Strategy Consulting

• Conduct thorough qualitative and quantitative research (for both scientific and non-scientific focused projects).
• Reach out and liaise with potential sites (e.g. hospitals, data holders) and stakeholders such as KOLs, Payers, Clients etc; for set up of contracts, project meetings, confidentiality agreements and applications.
• May serve as project manager on small-sized client engagements.
• Write and/or review data access applications to Nordic health data authorities (e.g. patient-level data, aggregate data requests).
• Conduct interviews with local clinical experts as well as with patients.
• Create well-structured, client-facing deliverables and communicate insights.
• Stay up to date on the national health data landscape in your country.
• May contribute to proposal development.

Consultant – Real World Solutions, Healthcare & Life Sciences

Software Engineer

• Program, validate, and deliver NONMEM‑ready PK/PD datasets based on SDTM/ADaM standards using advanced R programming skills
• Create high‑quality PK/PD datasets for both pre‑lock and post‑lock clinical data
• Independently execute programming tasks of medium to high complexity with excellent accuracy and timeliness
• Critically review data, identify inconsistencies or gaps, and propose solutions to improve dataset quality and programming efficiency
• Perform quality control (QC) of NONMEM datasets, including those produced by external partners
• Support preparation of deliverables for regulatory submissions following internal Pharmacometrics guidelines
• Conduct QC of customized R packages used for pharmacometrics workflows; enhance or build automated test suites where needed
• Liaise with cross‑functional teams including Data Management, Biostatistics, Statistical Programming, and Bioanalytical groups to resolve data issues and ensure alignment
• Adhere to relevant SOPs, working instructions, and regulatory standards; maintain inspection readiness
• Contribute as a technical driver in the development and improvement of new PM standardization initiatives related to dataset creation and QC.

PK/PD Statistical Programmer – homebased

Manager

• Draft sections of protocols, CRFs, training materials, and data review plans
• Contribute to the development of safety updates, IBs, and regulatory submissions
• Oversee data review and TMF audit readiness
• Forecast/manage investigational product supply
• Support study closeout, issue resolution, and lifecycle budget tracking
• Coordinate CRO/vendor selection and performance
• Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison

Global Trial Manager, Late Phase Studies

Director

• The leader of the cross-functional clinical trial team (CTT).
• Guides planning and management of the assigned clinical study/studies end-to-end.
• Executes and delivers clinical studies; guides planning and decision making.
• Acts as the CTT product owner with clear and focused duties.
• Promotes operational excellence in the shared development of global clinical study protocol(s).
• Responsible for proactive, iterative operational planning with effective contingencies.

Associate Director, Senior Study Lead – Single Sponsor Dedicated

Medical Director

• Provide medical, clinical, and scientific advisory expertise to all IQVIA divisions
• Serve as a Global Medical Advisor on assigned projects
• Provide medical support to investigative sites and project staff
• Review protocol-related issues including patient safety and eligibility
• Attend and present at Investigator Meetings
• Available 24/7 to respond to urgent protocol-related questions
• Requires regular travel (15%-20%)

Associate Medical Director, Cardiology – Metabolic Diseases and Nephrology

Pharmacist

• Advocate for patient safety and protocol integrity
• Compounds all IV doses of investigational products and conventional agents
• Maintains responsibility for the management of the inventory for protocols
• Orients IDS staff, pharmacy residents, and pharmacy students to the IDS pharmacy technician role
• Assist with monitoring visits and answering any monitor queries

Pharmacy Technician

Frontend Engineer

• Ensure comprehensive unit test coverage for all developed software
• Work closely with product and design teams to understand and implement requirements
• Contribute to the improvement of the development process and best practices

Senior Frontend Engineer

Analyst

• Assists with the review and analysis of client requirements or problems
• Assists in the development of detailed documentation and specifications
• Performs quantitative or qualitative analyzes to assist in identifying client issues
• Assists in the design and structure of presentations appropriate for the audience
• Develops a basic knowledge of consulting methodologies and the life sciences market

Analyst, EBP Analytics

• Review protocols, amendments, and study-specific documentation
• Verify dosing accuracy and oversee compounding of investigational products (IP)
• Maintain inventory and manage drug receipt and returns
• Supervise IDS technicians and support audits
• Orient new staff and maintain required certifications and licenses
• Upload and manage protocol documentation and staff credentials

Investigational Drug Services Pharmacist, On-site

Account Manager

• Recruit short-term acute care hospitals and Integrated Delivery Networks (IDNs) to participate in the IQVIA Hospital Data Exchange Program at no cost to the hospital.
• Present and educate hospital stakeholders on the value of the electronic Comparative Price Report (eCPR) and guide them through program participation requirements.
• Leverage recruitment tools to identify and engage appropriate purchasing and materials management leaders.
• Conduct outreach through written, phone, and virtual communications to secure hospital participation.
• Deliver virtual presentations and training sessions via Microsoft Teams; occasional travel may be required with approval.
• Provide timely support for technical inquiries related to FTP submissions, data formatting, and use of the IQVIA Customer Portal.
• Serve as a trusted point of contact for participating hospitals by clearly explaining how data is collected, validated, and used.

Account Manager – Hospital Data Services

Auditor

• Executes IT internal audit reviews and testing according to the annual IT Internal Audit plan, including fieldwork testing, documentation of results, and completion of workpapers in accordance with relevant internal and external auditing standards to determine adherence to guidelines and regulations and evaluate the effectiveness of internal controls.
• Supports the VP – Internal Audit, Audit Directors, and Audit Managers in delivering internal audit reviews.
• Assists in all audit processes, including risk assessment, planning, audit program development, execution of audit procedures, and communication of audit results and best practices to leadership.
• Determines compliance with IT policies and procedures.
• Performs analytical testing and review.
• Identifies internal control weaknesses and makes improvement recommendations.
• Performs Sarbanes-Oxley IT compliance work.
• Execute IC calculations at end of quarter.
• Develops and maintain effective working relationships with Internal Audit stakeholders.
• Assists in preparation of draft audit reports for management review.
• Participates in the continuous improvement of the Internal Audit department, including providing training and feedback related to audit activities.

Internal Auditor, Level 2

Data Engineer

• Lead the design of scalable data solutions
• Mentor talented engineers
• Work on projects that truly make an impact
• Build and optimize data pipelines that power forecasting and analytics platforms
• Collaborate with product managers, front-end and back-end developers, and fellow data engineers
• Ensure adherence to architectural standards
• Coach junior team members
• Maintain consistent coding standards across global engineering pods

Senior Data Engineer

• Support Practices to provide clinical tools and resource to help manage patients with long-term conditions.
• To ensure clinical services are delivered within the bounds of our protocols, service operating instructions and systems.
• To identify opportunities for clinical reviews at individual practice level, PCN or ICB level where there is clinical need.
• To enhance the awareness of Interface Clinical Services within primary care and to assist in developing long lasting relationships with practices and local NHS organisations.

Clinical Pharmacist

• Support the preparation, review, and maintenance of client contracts in accordance with IQVIA standards and processes.
• Collaborate with project teams (e.g., Project Management, Finance, Legal, Commercial) to determine appropriate contractual terms and conditions.
• Assist in negotiating, developing, and revising contracts, scopes of work, and associated budgets under guidance of senior team members.
• Ensure scopes of work are clearly defined and that budgets accurately reflect the agreed scope and services.
• Support the management of contract amendments and change orders, ensuring changes are integrated efficiently and accurately into the main study contract.
• Act as the primary customer interface for contractual matters on small to mid-size projects and provide support to senior team members on medium to large projects.
• Project-manage assigned contracting activities to ensure timely execution and completion of contracts.
• Maintain accurate and complete contract documentation and records in IQVIA systems and tracking tools.
• Identify issues or risks related to contract scope, timelines, or budgets and escalate appropriately.
• Participate in departmental initiatives, training activities, and continuous process improvement efforts.
• Perform other duties as assigned.