Role Overview In this role within the EMEA RW MEG you will be producing materials and services relating to the Health Economics Outcomes Research business areas (health economic modelling, evidence synthesis, statistical analysis, health technology assessment submissions, report and publication development for value communication) that generate value for our clients. The role of the Consultant is expected to play an important role in shaping the team’s literature review offerings. Responsibilities Shape and lead the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Review and senior leadership. Develop systematic literature methods, conduct searches in databases such as EMBASE, MEDLINE, Cochrane, PubMed, and use OVID SP or similar platforms. Stay current on methodologies and HTA requirements, acting as an in-house expert. Understand different types of literature reviews and manage projects with senior oversight. Guide the team on interpretation and qualitative synthesis of findings. Ensure literature reviews meet rigorous HTA requirements, conduct quality control of deliverables. Act as day‑to‑day contact with clients from pharmaceutical, biotechnology, and medical device companies in the EMEA region. Oversee development of research questions, PICOS criteria, search strategies, and review protocols. Contribute to business development and internal initiatives for innovative methods. Collaborate with other business areas and functions to deliver client services. Qualifications We are looking for a candidate with a good mix of academic and professional experience, domain experience and interpersonal skills. An ideal candidate has a good knowledge of literature review methods and has experience in conducting rigorous literature reviews in health sciences. The ideal candidate will also understand the typical structure of our pharmaceutical clients and how to navigate it to achieve client aims. Desired Skills and Qualifications Postgraduate degree or higher in a relevant discipline such as health, bioscience, medicine, biomedical sciences, health economics, health policy, epidemiology, public health or information science. Prior relevant experience, 2 years, including systematic literature reviews and/or meta‑analyses. Understanding of research principles, PRISMA, Cochrane guidelines, and bias assessment methods. Understanding of evidence‑based healthcare principles, critical appraisal and synthesis. Experience with HTA agency requirements for evidence reviews and synthesis. Excellent oral and written communication skills. Accuracy, attention to detail and time‑management skills. Knowledge of meta‑analysis methods is advantageous. Fluency in English with strong written and verbal communication. Commercial awareness and understanding of the pharmaceutical industry. Proficiency in MS Word, PowerPoint and Excel. Eligibility to work in one of our office locations without visa sponsorship. Benefits IQVIA offers numerous training opportunities, external trainings and conference attendance aligned with business objectives, unlimited access to eLearning courses, a competitive salary, bonus, benefits and flexible working options including remote work and occasional office visits. Application We welcome applications in English. #J-18808-Ljbffr