Job Description
Evidence Generation & IEP Lead - VC backed TechBio - London or Dubai (Hybrid)
A venture-backed TechBio company in London is hiring a senior-level evidence strategy expert to help shape the future of data-driven drug development.
You’ll join a team that’s rethinking the traditional model by building internal infrastructure, partnering directly with biotech & pharma, and embedding structured evidence planning into every stage of development.
This role blends scientific rigour with strategic oversight. It’s ideal for someone who thrives at the intersection of clinical development, real-world evidence, HEOR and regulatory strategy - and knows how to turn fragmented data into a coherent, execution-ready Integrated Evidence Plan (IEP).
Key Responsibilities
* Lead development and optimisation of Integrated Evidence Plans (IEPs) across assets and indications
* Conduct structured IEP gap analyses to identify evidence shortfalls across regulatory, HTA, payer and commercial stakeholders
* Align clinical development, RWE, HEOR and medical strategy into a unified evidence roadmap
* Advise internal teams and external partners on evidence sequencing and prioritisation
* Translate complex data landscapes into clear strategic recommendations
* Support protocol development and evidence generation frameworks to close identified gaps
* Engage with regulators and payers (where relevant) to ensure forward-aligned evidence planning
Ideal Candidate
* MSc/PhD in Epidemiology, Health Economics, Pharmacoepidemiology or related scientific field
* Significant experience in evidence generation strategy and IEP development within biotech or pharma
* Demonstrated expertise conducting formal IEP gap analyses across global markets
* Strong understanding of HTA and payer evidence expectations (UK, EU and/or US)
* Experience integrating RWE, clinical development data and health economic endpoints
* Confident engaging cross-functionally with Clinical, Regulatory, Market Access and Commercial teams
* Ability to move between high-level strategy and practical implementation
Bonus Experience
* Prior experience in a startup, CRO, techbio or agile biotech environment
* Exposure to early asset strategy through to launch
* Experience supporting global evidence submissions or parallel regulatory/HTA pathways
* Familiarity with structured evidence planning frameworks or digital evidence management tools
This is an opportunity to join a company that’s not just running studies - but architecting how evidence is planned, prioritised and delivered in modern drug development.
If you combine strategic evidence leadership with hands-on execution and cross-functional credibility, we’d love to speak.
London or Dubai (2 days per week)
£75,000 - £110,000 p/a
Unlimited holidays + equity