Systematic Literature Reviewer hybrid

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.

• Shape and lead the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Review and the wider senior leadership team
• Develop searches in various databases (e.g., EMBASE, MEDLINE, Cochrane, Pub Med) and use platforms such as OVID SP
• Stay up to date on new methodologies and HTA requirements for systematic literature reviews and act as an in-house expert for the team
• Understand different types of literature reviews (systematic, targeted, pragmatic, etc.)
• Manage literature review projects with senior oversight
• Guide interpretation and qualitative synthesis of literature review findings
• Oversee literature review projects that meet rigorous HTA requirements; conduct quality control of deliverables (searches, screening, data extraction, reporting)
• Serve as day-to-day contact with clients in the pharmaceutical, biotechnology and medical devices sectors within the EMEA region, with senior oversight
• Oversee development of research questions, PICOS criteria, search strategies and literature review protocols
• Contribute to business development and internal initiatives for advancing methodological approaches
• Collaborate with other business areas and functions to deliver client services and support the development of new offerings

We are looking for a candidate with a mix of academic and professional experience, domain experience and interpersonal skills. An ideal candidate has knowledge of literature review methods and experience conducting rigorous literature reviews in health sciences. The candidate should understand the typical structure of clients in the pharmaceutical industry and how to navigate this structure to achieve client aims.

• Postgraduate degree or higher in health, bioscience, medicine, biomedical sciences, health economics, health policy, epidemiology, public health, or information science
• Prior relevant experience, 2+ years (e.g., systematic literature reviews and/or meta-analyses)
• Understanding of PRISMA, Cochrane guidelines for SLRs, and risk-of-bias assessment methods
• Understanding of evidence-based healthcare principles, critical appraisal, and synthesis of health care research
• Understanding (and experience is advantageous) with HTA agency requirements for evidence reviews and synthesis
• Excellent oral and written communication skills
• Attention to detail and time management
• Understanding of meta-analysis methods is advantageous but not essential
• Fluency in English; strong written and verbal communication
• Commercial awareness of the pharmaceutical industry is advantageous
• Proficiency with MS Word, PowerPoint, Excel
• Eligibility to work in one of our office locations without visa sponsorship

Please submit your CV in English.

IQVIA offers opportunities for professional growth in the healthcare industry. You will join a team of 90+ professionals with diverse disciplines. New joiners may be paired with a more experienced colleague in a buddy system during the first months. IQVIA provides training opportunities, external trainings and conference attendance aligned with objectives, and access to eLearning courses and internal training. The role offers a competitive salary, bonus and benefits, with flexibility including remote working and occasional office visits.