For over thirty years, Cytel has enabled the world’s biotech and pharmaceutical companies to make confident, evidence-based decisions to ensure successful outcomes. As industry leaders in delivering advanced data analytics solutions, we continually invest in deepening our expertise. Now, we have a fully integrated Evidence Value & Access business, with a global team of experts providing industry-leading capabilities in market access, health economics and outcomes research (HEOR) and real-world evidence (RWE).

Powered by the unique experience and expertise of our researchers and consultants around the world, we conceptualize and execute HEOR and RWE studies, using advanced quantitative techniques to prepare sponsors for reimbursement submission and to support a product’s clinical and economic value proposition. Our mission is to help unlock the full promise of data – our teams conduct evidence generation and synthesis, economic analyses, and comparative effectiveness studies to generate the evidence to support the overall product value, with our Access team acting as the evidence hub by which we devise strategy and translate evidence into concise value propositions and communications for payers and other external stakeholders.A scientific/strategic contributor with broad expertise and/or unique knowledge in a specific area, and an ability to achieve objectives in creative and effective ways. Typically manages multiple projects within a client or within a specialized area across several clients.

Responsible for independently (most of the time) leading projects (up to 5-6 mid-size projects) involving literature reviews,



including systematic literature reviews (SLRs) on various topics and indicationsAs project lead, responsible for client communication, overall project management and operations, coordination of project day-to-day activities, and quality of deliverablesProvide senior-level quality review and methodological guidance to junior team members, supporting technical capability development and ensuring consistent scientific rigor across project deliverablesResponsible for conducting and leading HTA-compliant and EU-JCA compliant SLR packagesMaster 80% of the techniques used in his/her specialtyCollaborates closely with other senior members to determine to support business development activities, such as proposal development, project scoping, capabilities/demo presentationsResponsible for line management and mentoring of 1-2 junior research consultants or research associatesQualifications Master’s degree in Pharmacology, Biochemistry, Epidemiology, Health Economics or other relevant scientific field. PhD or MD highly desirable.Experience: 4-5 years of experience at a minimum in the clinical trials or health research or consulting setting. Comfortable presenting and interfacing with senior executives within the clients.

Strong technical writing, oral communication and presentation skills, excellent use of the English language.Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law. #

📌 Senior Research Consultant, Evidence Synthesis (Winnipeg)
🏢 Cytel
📍 Winnipeg