IQVIA

Research Analyst

• Working in partnership with a single-sponsor.
• Usually allocated to 1-2 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes).
• Responsible for approximately 10 sites.
• On site between 6 and 8 days per month, dependent on the sponsor.
• All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager.
• Permanent employment contract.
• Sponsor model has reduced travel (approx. 30% or less) due to using the Risk Based Monitoring which incorporates remote monitoring therefore there is less need for on-site visits.

Junior Clinical Research Associate – Sponsor-dedicated

Medical Director

• Provide medical, clinical, and scientific advisory expertise to all IQVIA divisions
• Participate in all aspects of Medical Science involvement on assigned trials
• Serve as a medical expert during project delivery lifecycle
• Provide therapeutic and medical expertise to business development activities

Associate Medical Director – Rheumatology

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

Account Manager

• Serve as the primary point of contact for assigned Small Pharma accounts, owning overall client relationship health and satisfaction.
• Manage day-to-day client interactions, including scope management, expectation setting, issue resolution, and escalation mitigation.
• Proactively identify opportunities to reshape scope, reframe client needs, and expand engagement value.
• Promote and sell IQVIA data assets and broader commercial solutions to existing clients through value-based, consultative conversations.
• Identify new revenue opportunities within assigned accounts and support value-added sales initiatives.
• Partner with internal sales specialists and solution teams to bring the right offering to each client.
• Own contracting, invoicing, and commercial administration for assigned accounts.
• Coordinate closely with cross-functional teams (Sales, Delivery, Analytics, Legal, Finance, etc.) to ensure seamless execution and service delivery.
• Broker appropriate internal support across the broader IQVIA network based on client needs.
• Host and participate in internal business reviews and account planning sessions.
• Represent IQVIA at client meetings, conferences, and IQVIA-sponsored events.
• Build trusted relationships with client stakeholders while positioning IQVIA as a long-term strategic partner.

Account Manager, Small Pharma

• 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

• 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.