Job Description
Systematic Literature Review Scientist - Midsized Healthcare Consultancy Full remote flexibility / the choice of UK office locations. Base salary £40,000 - £55,000 + bonus & benefitsCompany:An employee owned, global leader in technology-led, medical affairs, HEOR and value communications, we are a full-service medical communications agency that partners with pharmaceutical, life science and biotech companies around the world to bring new healthcare treatments to market, ultimately making the world a healthier place.Be part of a broad HEOR and market access offering to clients across multiple aspects of product value, including evidence generation planning, evidence reviews (SLR/REA), global payer landscape, global value message development, global pricing, value communications and HEOR publications.The role:As a Systematic Literature Review (SLR) Lead, you will work on a variety of programs focused on the demonstration of product value. Core activities will include conducting HTA (NICE in particular) compliant SLRs, developing and running literature database searches, data evaluation and extraction, report writing, database management, proposal development, and client relationship building.Key responsibilities:• Support in all aspects of SLRs, rapid evidence assessments, and targeted literature reviews including liaising directly with clients.• Drafting of needs assessments and project proposals to a high standard.• Research plans, project timelines, research outputs, and key deliverables with a strategic focus.• Conduct SLRs and other evidence reviews including producing formal reports for clients.• Collaboration with HEOR writers to develop articles for submission to journals and submission to scientific congresses.Skills and experience required:• Ideally qualified to PhD level in Health Sciences field.• Demonstrable experience of leading and developing SLRs including to support HTA submissions, ideally in a Consulting/Private sector setting.• Knowledge and experience with SLR best practices and guidelines, including HTA evidence review group expectations.• Knowledge of the pharmaceutical industry, drug development process, and global payer environment.• Understanding of clinical data, real-world evidence, and cost-effectiveness assessments.• SLR software experience - preferred.• Ideally familiarity with meta-analysis and network meta-analysis/indirect treatment comparisons.• Effective project management experience.• Rigorous attention to detail.What's in it for you?• Excellent career growth and mentorship• Learning and development opportunities, including a personalised leadership program• Flexible working arrangements that facilitate a strong work-life balance• Competitive compensation package with annual performance and salary reviews• Medical, dental, and vision coverage from your first day• Share ownership program• An environment that promotes collaboration where employees have a voice, the space to invent, the chance to excel, and to have fun!Contact me now for more info: greg.harris@evisci.com