Specialist drug development consultancy
oncoKnow provides deep, specialist knowledge across drug development — with a particular focus on oncology and rare disease, and broad experience across other therapeutic areas.
What we do
With a primary focus on oncology and rare disease, and experience spanning broader therapeutic areas, we bring the depth and versatility that complex drug development programmes demand.
Designing research backwards from patient, label and access, identifying translational gaps early across biology, clinic, CMC and regulation, and making preclinical data regulatory-fit, not just publication-fit.
How the pipeline actually connects, spotting warning signs before FIH, PoC or MAA, aligning discovery, clinical, regulatory and CMC timelines, and knowing when not to advance a programme.
Trials designed to answer both regulatory and value questions, balancing protocol trade-offs with real-life feasibility, with deep experience in early-phase rare disease and oncology and productive interfaces with CROs, sites and regulators.
Understanding how regulators think, not just what they ask for, briefing book narrative and strategy, knowing when to engage and when not to, across EMA, FDA and national authorities.
Tailoring data for regulators, investors, clinicians and boards, KOL advisory board design and moderation, and scientific storytelling that survives scrutiny.
Our approach
We immerse ourselves in your compound, indication, and competitive landscape to understand what truly differentiates your programme.
Drawing on decades of oncology experience, we co-create development strategies that are scientifically rigorous and commercially aware.
We stay alongside your team through implementation, providing expert guidance at every regulatory, clinical, and scientific milestone.
About oncoKnow
oncoKnow is founded by Nadina Grosios, PhD, MPH. Her driving ambition is to support teams working on innovative therapies and help bring those therapies as close and as accessible to patients as possible.
Over the past 20+ years she has worked across the full drug development pipeline reaching milestones from first-in-human through to Marketing Authorization. Her career spans laboratory leadership and translational science at Novartis and AstraZeneca, coordination of multidisciplinary academic research and health initiatives at the University of Leeds, NHS and Cancer Research UK, project leadership at uniQure, and consulting and clinical operations at SMS-oncology.
Since founding oncoKnow in 2018, she has helped multiple teams think translationally, decide wisely, and move therapies through real-world complexity without losing scientific integrity, or time.
Get in touch
Whether you're at preclinical stage or preparing for approval, we'd love to understand your needs.