Senior Systematic Literature Review Specialist

4 semanas atrás

Porto Salvo, Lisboa, Portugal IQVIA Tempo inteiro

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Our company creates intelligent connections across all aspects of healthcare through our analytics, transformative technology, big data resources, and extensive domain expertise.

Within the Real World Solutions (RWS) group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 90 highly qualified multi-disciplinary professionals from various disciplines, including health economics, statistics, epidemiology, and data management, located across 8 geographies.

Our clients operate in the life sciences industry, including the global top 20 pharmaceutical companies, medical device, and biotech companies, as well as public health providers and regulatory authorities. Our clients seek insight and evidence on the safety, efficacy, effectiveness, and cost-effectiveness of healthcare delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas.

For this role within the EMEA RW MEG team, you will be producing materials and services relating to the Health Economics Outcomes Research business areas, generating value for our clients. You will primarily use systematic and non-systematic literature review methodology, such as targeted literature review. The role of the Analyst/Consultant is expected to play an important role in shaping the team's literature review offerings.

The role is located in Lisbon or Athens, with flexibility regarding frequency of office and home working. Please refer to our diversity and inclusion statement for further information.

Key Responsibilities:

  • Shaping and leading the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Reviews and the wider senior leadership team
  • Developing searches in various databases and proficiently using OVID SP or another similar platform
  • Overseeing the development of research questions, PICOS criteria, search strategies, and literature review protocols
  • Keeping up to date on new methodologies and HTA requirements for systematic literature reviews and being an in-house go-to expert for the team
  • Managing literature review projects with senior oversight
  • Guiding the team on interpretation/qualitative synthesis of the literature review findings
  • Overseeing literature review projects that meet rigorous HTA requirements, conducting quality control of literature review deliverables
  • Being a day-to-day contact with clients, including pharmaceutical, biotechnology, and medical devices companies with global and regional headquarters based in the EMEA region
  • Contributes to business development as well as internal initiatives for the advancement of innovative methodological approaches
  • Collaborating with other business areas and functions of the organisation to deliver client services and support the development of new offerings

Qualifications and Desired Experience:

  • Excellent knowledge of literature review methods and experience in conducting rigorous systematic literature reviews in health sciences, from start to finish
  • Having completed one or more systematic literature review projects, adherent to quality standards (e.g. PRISMA, Cochrane), with at least one relevant scientific publication is a strong asset
  • Good understanding of the typical structure of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve client's aims

Desired Skills and Qualifications:

  • Excellent understanding of research principles, PRISMA principles, Cochrane guideline for SLRs, methods of the assessment of risk of bias for different study designs
  • Prior relevant experience, > 2 years (ideally on one or more systematic literature reviews and/or meta-analyses projects)
  • Postgraduate degree level education or higher from a relevant discipline such as health or bioscience-related, medicine, biomedical sciences, health economics, health policy, epidemiology, public health, or information science
  • Understanding of meta-analysis and indirect treatment comparison methods is advantageous, but not essential
  • Understanding of the principles of evidence-based healthcare, critical appraisal, and the interpretation and synthesis of health care research
  • Understanding (and experience is advantageous) with the HTA agency requirements for evidence reviews and synthesis
  • Excellent oral and written communication skills with fluency in English
  • Accuracy, attention to detail, and time management skills
  • Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry is advantageous
  • Proficiency in MS Word, PowerPoint, Excel
  • Eligibility to work in one of our office locations without visa sponsorship

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