Rwe/heor Consultant

With approximately 85,000 employees in more than 100 countries, IQVIA is in a truly unique position to be able to support companies seeking to improve real-world patient outcomes and enhanced clinical trial outsourcing through treatment innovations, care provision and access. With a broad range of healthcare information, technology and service offerings, IQVIA provides solutions that span clinical to commercial, bringing clients an exceptional opportunity to realize the full potential of innovations and advance healthcare outcomes.
- The context:

- As an Analyst within the Real World Evidence Department, you will have a key role to support the HEOR practice. You are expected to be able to work in different projects for different clients on the Portuguese market. You will carry out your tasks to a high standard which meets or exceeds the client's expectations. You will support senior staff on specific business initiatives.
- The missions:
- Assist with overall project/client management-
- Attend client and other external meetings as appropriate-
- Manage specific project work streams independently-
- Develop search strategies for structured and systematic literature reviews-
- Manage the full review process (abstract review, paper selection and data extraction)-
- Write and review literature review reports-
- Help in designing data collection forms, known as case report forms (CRFs)-
- Coordinate with local ethics committees,-
- Identify/select investigators responsible for the conduction of site studies-
- Ensure that investigators and the sites where the research is to be performed are adequate to the purposes of the study-
- Liaise with doctors/consultants or investigators and obtain compromise before sending the study materials-
- Monitor the study throughout its duration, (which involves visiting or contacting the study sites on a regular basis, or performing remote monitoring activities)-
- Ensure that storage, distribution, return procedures and documentation for the study are secure and adequate-
- Manage CRFs files (verify consistency with patient clinical notes ect)-
- Perform follow up on Data Management or SAE (safety) queries-
- Send regular study reports to concerned stakeholders-
- Closing down study sites on completion of the study-
- Archiving study documentation and correspondence-
- To coordinate investigator payment-
- Occasionally manuscripts for publication- The profile:
- MHA/MPH/PhD - education in Health Science, Public Health, Health Services Research (or a related area)-
- Clinical trials monitoring knowledge or experience-
- Around 3 years of work experience in outcomes research/RWE/evidence generation-
- Strong qualitative and quantitative skills-
- Excellent command of Portuguese, and good English are required-
- Self-driven approach, and ability to work in teamIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at