FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
About the role
Key responsibilities & impact- Design, deliver, and interpret evidence review projects for pharmaceutical and healthcare clients across therapeutic areas.
- Manage and deliver systematic and targeted literature reviews, evidence landscape assessments, and evidence reviews supporting HTA submissions, EU Joint Clinical Assessments, indirect treatment comparisons, publications, and other evidence-generation activities.
- Shape and critically review research questions, PICOs, eligibility criteria, protocols, data extraction frameworks, quality assessment approaches, and evidence synthesis plans.
- Provide senior methodological input on evidence quality, relevance, and applicability, identifying limitations, inconsistencies, evidence gaps, and implications for HTA, JCA, downstream analyses, and client decision-making.
- Synthesise findings across studies and evidence sources and translate results into conclusions and recommendations for client reports, presentations, workshops, publications, and other scientific deliverables.
- Manage evidence review workstreams, coordinating timelines, deliverables, and junior team members.
- Contribute to client meetings and workshops, presenting findings and discussing methodological considerations and implications.
- Provide senior quality review and methodological guidance to junior team members.
- Collaborate with statistical colleagues on indirect treatment comparison feasibility assessments, network meta-analysis, MAIC, and STC.
- Maintain knowledge of evidence synthesis, HTA, and JCA methodological developments.
- 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.
Benefits
Comp & perks- Competitive salary
- Bonus
- Pension
- Private Healthcare
- Dental Cover
- Enhanced Eye Care Cover
- Electric Car Scheme
- Staggered working hours
- Occasional travel to attend client meetings in person or conferences