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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in evidence synthesis, systematic review methodology, and health technology assessment (HTA) requirements, with a strong ability to manage projects and mentor junior team members. Proficient in translating complex evidence into actionable insights for pharmaceutical and healthcare clients.
Highest-signal resume keywords
Evidence SynthesisSystematic Review MethodologyHealth Technology Assessment (HTA)Project ManagementClient Engagement
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Literature ReviewData Extraction FrameworksQuality Assessment ApproachesIndirect Treatment ComparisonNetwork Meta-AnalysisMAICSTCStatistical AnalysisEpidemiologyBiostatistics
Soft Skills
CollaborationCritical ThinkingCommunicationMentoringProblem Solving
Certifications & Qualifications
Master's DegreePhD
Industry Keywords
PharmaceuticalHealthcareConsultancyCROPublic Health
About the role
Key responsibilities & impact- Design, deliver, and interpret evidence review projects for pharmaceutical and healthcare clients across therapeutic areas
- Manage evidence synthesis projects and major workstreams, including systematic and targeted literature reviews
- Deliver evidence assessments supporting HTA and EU Joint Clinical Assessments (JCA)
- Conduct reviews supporting indirect treatment comparisons, publications, and broader strategic evidence-generation activities
- Take responsibility for scientific quality and day-to-day delivery of assigned projects and workstreams
- Apply methodological judgement to complex evidence questions, identify evidence gaps and limitations, and translate findings into conclusions and recommendations
- Collaborate with evidence review, statistics, health economics, epidemiology, and other disciplines
- Provide senior review and guidance to junior team members
- Shape and critically review research questions, PICOs, eligibility criteria, protocols, data extraction frameworks, quality assessment approaches, and evidence synthesis plans
- Synthesise findings across studies and evidence sources for reports, presentations, workshops, publications, and scientific deliverables
- Coordinate workstream timelines, deliverables, and junior team members
- Contribute to client meetings and workshops, presenting findings and discussing methodological considerations
- Work with statistical colleagues on indirect treatment comparison feasibility assessments, network meta-analysis, MAIC, and STC
- Maintain knowledge of evidence synthesis, HTA, and JCA requirements
- Contribute to proposals, scopes of work, budgets, business development, and internal methodological development
- Support Lumanity's AI-enabled evidence review approaches with scientific judgement and quality-control processes
Requirements
What you’ll need- Master's degree or PhD in epidemiology, pharmaceutical sciences, public health, biostatistics, or another relevant health sciences discipline
- 5+ years of relevant professional experience in evidence synthesis
- Substantial hands-on experience independently managing systematic and targeted literature reviews from protocol development through evidence synthesis, interpretation, and reporting
- Strong understanding of systematic review methodology and relevant methodological guidance
- Ability to identify and resolve methodological issues with limited senior oversight
- Strong experience critically appraising and synthesising complex evidence and translating findings into clear conclusions, recommendations, and implications for clients
- Experience managing defined projects or major workstreams, including coordination of timelines, deliverables, and junior team members
- Experience engaging in client meetings, presenting findings, and discussing methodological or strategic considerations with senior stakeholders
- Working knowledge of HTA requirements across major markets, including the EU HTA Regulation and Joint Clinical Assessment requirements
- Experience with indirect treatment comparison feasibility assessments and familiarity with network meta-analysis, MAIC, and STC is desirable
- Experience contributing to proposals, business development, or client account development is desirable
- Relevant experience ideally within a consultancy, CRO, pharmaceutical company, or similar environment
- Occasional travel may be required, for example to attend client meetings in person or conferences
Benefits
Comp & perks- Competitive salary
- Bonus
- Pension
- Private Healthcare
- Dental Cover
- Enhanced Eye Care Cover
- Electric Car Scheme
- Staggered working hours