About F-MAC — Senior European Medical Affairs Expertise Delivered Flexibly
About F-MAC
Senior European Medical Affairs expertise, founder-led
F-MAC is a specialist European Medical Affairs consultancy
supporting clinical-stage biotechnology companies developing
medicines across Europe.
Founder-led by Dr Lee Finlan, F-MAC provides senior involvement from
strategy through hands-on field execution, with support scaled to the
needs and stage of each programme.
Lee is a PhD-trained cancer scientist and experienced European Medical
Affairs leader whose career spans oncology research, clinical development
and field medical leadership.
His specialist experience includes pancreatic cancer (PDAC), non-small cell lung cancer (NSCLC), metastatic colorectal cancer (mCRC) and acute myeloid leukaemia (AML), with particular depth in precision oncology and RAS/KRAS-targeted drug development.
A flexible model proven in practice
Lee's industry career has included both outsourced and directly employed European Medical Affairs leadership.
He first worked through Amplity in outsourced Field Medical roles and subsequently led European programmes supporting Halozyme and Mirati Therapeutics. In both cases, the outsourced assignment progressed into a direct Senior Director position with the client. Being retained and appointed directly into senior leadership roles from the outsourced model — twice — provides Lee with first-hand experience of how flexible Medical Affairs capability can support a growing
biotech before permanent European infrastructure is fully established.
It is an operating model F-MAC understands from both sides.
I previously held European Medical Lead and Senior Director roles at Mirati Therapeutics and Halozyme Therapeutics, leading European field medical teams and contributing to global medical strategy.
Through F-MAC, I have supported clinical-stage precision-oncology companies developing RAS(ON), menin and PRMT5 inhibitors. My work spans Phase I–III development, investigator engagement, clinical trial support and pre-launch preparation.
Through F-MAC I have supported European clinical development and field medical activity for emerging
precision-oncology companies. This has included a clinical-stage developer of RAS(ON) inhibitors, supporting its wider pipeline across Europe at critical stages ahead of its European build-out, as well as a menin inhibitor programme in oncology and a PRMT5 inhibitor programme. The work involved investigators, KOLs, clinical centres and global cross-functional teams across Europe, connecting scientific strategy with practical field
execution and supporting trial recruitment.
Start with what you need. Scale when you need it.
F-MAC brings together three capabilities particularly relevant to clinical-stage biotech:
Scientific Depth
PhD-level scientific grounding in the field p53, cancer stem cells and epigenetics combined with extensive
experience interpreting emerging oncology and clinical data.
European Field Experience
Hands-on engagement with investigators, KOLs and leading clinical centres across European markets.
Senior Medical Affairs Judgement
Pragmatic support informed by experience spanning Field Medical, Clinical Development and European Medical Affairs leadership.
F-MAC is deliberately flexible. Support can range from a defined project or fractional leadership requirement through to Field Medical and broader outsourced European capability.
Research Background
Before moving into industry, Lee built his career in academic cancer research.
His early research at The Christie Hospital, Manchester included receptor and biomarker immunohistochemistry in breast cancer, including ER, PR, EGFR and HER2. He subsequently completed a British Skin Foundation-funded PhD at the University of Dundee, investigating UV-dependent regulation of the p53 tumour suppressor pathway. The University of Dundee records the three-year studentship and Lee's award of the PhD for this research. His work during this period contributed to peer-reviewed research on p53 signalling,
phosphorylation and cancer biology.
Lee later became an MRC Career Development Fellow at the MRC Human Genetics Unit in Edinburgh, where his research extended into p53/p63 biology, cancer stem-cell biology and genome organisation. Contemporary publications explicitly identify him as an MRC Career Development Fellow.
This scientific grounding continues to shape F-MAC's approach: understanding the underlying biology, critically interpreting emerging evidence and engaging investigators on the science behind a clinical programme — not simply communicating prepared messages.
Lee's transition into industry was recognised early in his Medical Affairs career, including recognition in the
Bronze Medal - PharmaTimes MSL of the Year competition in 2014, alongside further recognition during
subsequent Field Medical roles.
Discuss Your European Medical Affairs Needs
Whether you require a focused project, European Field Medical capability or senior fractional support, F-MAC would be pleased to discuss your programme.
That combination gives F‑MAC a deep understanding of translational science, trial design and regulatory
context, plus hands‑on experience engaging with healthcare professionals and shaping evidence
generation and medical strategies in real world and commercial settings.
Clients work with F‑MAC to benefit from strategic
scientific insight, clear clinical perspectives and
pragmatic execution informed by frontline medical
affairs experience across Europe.
Start with what you need. Scale when you need it

What makes F-MAC different
Scientific depth, European field experience and senior Medical Affairs judgement
F-MAC – Finlan Medical Affairs Consultancy Ltd brings together three strengths that matter to clinical-stage biotech:
1. Deep scientific expertise
2. Hands-on European field experience
3. Senior Medical Affairs judgement
We translate complex science into practical,
stakeholder-focused plans and deliverables, ensuring evidence and strategy are aligned with real-world
clinical and commercial needs. Our approach is
pragmatic and proportionate. We provide experienced support tailored to the scale and stage of your
program, avoiding one-size-fits-all solutions. Whether you need strategic advisory, field team design, clinical engagement, or phase-appropriate medical planning, our recommendations are implementable, risk-aware and designed to preserve your resources while
accelerating development goals. Working with seasoned Medical Affairs leaders who have operated across European markets means you get actionable insight informed by regulatory nuance, local practice patterns and payer landscapes. We partner closely with internal teams to prioritize what matters most for clinical development and market readiness, always
focused on clear, measurable outcomes.

Scientific Integrity
We prioritise rigorous scientific analysis and evidence led decision making in all our recommendations.
Client Partnership
Building trusted, collaborative relationships with biotech leaders to deliver tailored consultancy services.
Strategic Insight
Combining deep clinical knowledge with market understanding to craft impactful medical affairs strategies.
Come and Speak to us.
Engage with F-MAC’s senior team to explore how our evidence-led consultancy can augment your medical affairs and clinical development.
