Senior Research Consultant leading systematic literature reviews and HTA-compliant evidence packages for Cytel’s biopharma analytics business. Managing clients, deliverables, junior researchers, and business development.
Responsibilities
Independently lead up to 5–6 mid-size projects involving literature reviews, including systematic literature reviews (SLRs)
Serve as project lead for client communication, project management, operations, day-to-day coordination, and deliverable quality
Provide senior-level quality review and methodological guidance to junior team members
Support technical capability development and consistent scientific rigor across deliverables
Conduct and lead HTA-compliant and EU-JCA-compliant SLR packages
Master 80% of techniques used in the specialty
Support business development activities, including proposal development, project scoping, and capabilities/demo presentations
Line-manage and mentor 1–2 junior research consultants or research associates
Act as the client’s primary point of contact and develop mutually beneficial client partnerships
Requirements
Master’s degree in Pharmacology, Biochemistry, Epidemiology, Health Economics or another relevant scientific field
Minimum 4–5 years of experience in a clinical trials, health research, or consulting environment
Additional experience may be required depending on focus area
Thorough understanding of the biopharmaceutical R&D process and business acumen
Comfortable presenting and interfacing with senior client executives
Strong technical writing, oral communication, and presentation skills
Excellent use of the English language
Interest in and familiarity with AI for literature review, including published guidelines
Ability to work effectively in a demanding, challenging, rapidly changing environment
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