At Orakl Oncology, we are accelerating the development of oncology treatments. Today, fewer than 5% of new cancer drugs succeed in clinical trials. Clearly, new methods are needed. We combine cutting-edge biology and AI to build the next generation of insight platforms with the world's largest cohort of patient tumor avatars. These avatars fuel our AI-powered predictive engine, helping to anticipate clinical trial outcomes, validate therapies, and uncover new drug candidates. By generating multimodal, real-world data, we deliver insights that consistently outperform existing solutions.
Our mission is simple yet ambitious: to bring more effective treatments to patients who need them - and to make drug development smarter, faster, and more personalized. We collaborate with top hospitals, research institutes, and pharmaceutical companies worldwide. Backed by leading investors, we are a fast-growing, mission-driven startup at the intersection of science and technology.
The roleOur clinical-prediction offer gives pharma partners the evidence to guide decisions before and during clinical development. We are looking for a Scientific Product Director to turn this science into sellable products: decide what gets developed and when, define what each capability can claim and output, and shape how results are delivered to partners.
You will report to Gustave Ronteix, CTO and co-founder, and work daily with a tight-knit interdisciplinary team composed of Computational Biology, Data Science, R&D, Platform Strategy & Operations, BD and Pharma Partnerships.
What you'll doDesign and build a scalable product capable of derisking and accelerating clinical development of drug candidates based on Orakl’s scientific capabilities
Turn signals from BD, Pharma Partnerships and R&D into capability definitions: specs, target metrics, validation plan, cost to deliver, etc.
Set priorities and timelines with the internal teams
Identify productization-gaps, quality issues and feed back the ajustements into the product roadmap
Maintain the capability catalog: help guide scientists and researchers to what we can do
Own the product delivery gates: for each novel capability and product improvement, design the QC and validation steps
Oversee the scientific case for each capability: white papers, application notes, posters
Design the reports, data packages and dashboards partners receive, and direct the engineers who build them
PhD or equivalent in cancer biology, pharmacology, biostatistics or computational biology
8+ years in translational oncology, biomarker or diagnostics development, computational-biology platforms or preclinical CRO services, including 2+ owning a product roadmap
Technical depth: you read and understand production code, and can brief and review the work of engineers who build our reports and dashboards
You can judge evidence: from a validation pack, and this is backed by strong quantitative skills
You have experience working at the intersection of scientific and business departments within fast-growing companies
You know how pharma operates: you have contributed to proposals, SOWs and due-diligence questions, and know what a go/no-go decision by pharma requires
Fluent in English
You have seen bespoke research work turned into something repeatable and sellable
Scientific authorship: Posters, talks, papers or white papers; a presence at AACR, ASCO, ESMO or SITC
Regulatory: exposure to regulated or quality-managed environments
Mission: work on the forefront of cancer research
Ownership: a product function to build from the ground up
Impact: pharma teams make real portfolio decisions with what you define
Team: an exceptional crew of clinicians, biologists, engineers and data scientists, most with a PhD
Intro call (30 min) with Gustave Ronteix, CTO
Technical interview (1h)
On site case study followed by conversations with BD, Pharma Partnerships, the Engineering / Data Science leads and Platform Strategy & Operations
References: 2-3, including a direct manager
Skills Required
- PhD or equivalent in cancer biology, pharmacology, biostatistics, or computational biology
- 8+ years of experience in translational oncology, biomarker or diagnostics development, computational-biology platforms, or preclinical CRO services
- At least 2 years owning a product roadmap
- Ability to read and understand production code and review engineering work for reports and dashboards
- Ability to evaluate validation evidence and determine scientifically supported claims
- Experience working across scientific and business departments in fast-growing companies
- Knowledge of pharmaceutical proposals, statements of work, due diligence, and go/no-go decision requirements
- Fluent English
- Experience productizing bespoke research into repeatable, sellable offerings
- Scientific authorship, including posters, talks, papers, or white papers
- Conference presence at AACR, ASCO, ESMO, or SITC
- Exposure to regulated or quality-managed environments
- Therapeutic or preclinical knowledge in ADC, immuno-oncology, targeted therapy, organoids, or in-vitro pharmacology
- Clinical-trial design or trial statistics experience
- Experience with templated reporting, report-generation frameworks, or web front-end development
What We Do
Orakl Oncology is a techbio startup and precision oncology company that combines cutting-edge biology and AI to accelerate cancer drug discovery and development. Utilizing an innovative predictive engine and one of the world's largest collections of patient tumor avatars, the company aims to de-risk clinical trials, identify new drug targets, and expand the therapeutic arsenal available to cancer patients.









