PbHAYS /b is partnering with a bTop 10 global pharmaceutical company /b operating across more than b60 countries and 5 continents /b. /ppbr/ppThe company develops innovative medicines for bhuman and animal health /b and has established a bDigital Hub in Sant Cugat del Vallès /b to support international, data‑driven projects across the group. /ppbr/ppWe are looking for a bSystematic Literature Review Writer /b who will lead the bdesign, execution, and delivery of high‑quality literature reviews and evidence syntheses /b, collaborating with cross‑functional stakeholders to support bevidence generation across multiple therapeutic areas /b. /ppbr/ppbKey Responsibilities /b /pulliProvide expertise in designing, executing, and managing literature review services, including systematic literature reviews, meta-analyses, and targeted literature searches. /liliRefine literature review questions in alignment with project lead and prepare research protocols. /liliDesign literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites). /liliScreen abstracts and full-texts to determine relevance based on PICO criteria. /liliCritical appraisal to assess study quality, risk of bias, and heterogeneity to determine suitability for inclusion. /liliCreate and review PRISMA diagrams to document full-text study selection. /liliExtract and synthesize data from included articles into predefined templates, performing meta-analyses where appropriate. /liliDraft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends. /liliEnsure quality and accuracy of assigned work. /li /ulpbr/ppbRequirements /b /pulliAdvanced degree (PhD, Master’s, or Bachelor’s) in a relevant scientific field, with 3+ years (PhD/Master’s) or 5+ years (Bachelor’s) of experience in systematic literature review methods in the pharmaceutical, biotech, or consulting setting. /liliExperience conducting different types of literature reviews (clinical, economic, QoL, burden of illness, etc.) and meta-analyses. /liliExperience using statistical software (e.g., RevMan, Stata, R, Comprehensive Meta-Analysis) to conduct meta-analyses, generate forest plots, and calculate pooled estimates. /liliProficiency in biomedical databases (e.g., MEDLINE, Embase) and systematic review tools. /liliStrong organizational skills with the ability to manage multiple projects and deadlines. /liliSkilled in reference management tools (e.g., EndNote, Readcube) and Microsoft Office suite. /liliExcellent attention to detail, communication skills, and ability to work both independently and collaboratively. /liliPrior experience working in any of the therapeutic areas of Cardiovascular Renal Metabolism (CRM), Respiratory, Inflammation, Immunology, Oncology would be advantageous /li /ulpbr/ppbWhat do we offer? /b /pulliWorking with a Top pharma company- Opportunity to develop a multinational career /liliLong-term project. Permanent contract with Hays to provide customer service. /lilibOne office day per month /b. Transit included – buffet onsite. Location: Barcelona (Sant Cugat del Vallès) /li /ul