UzcaTech AB
UzcaTech AB
Hands-on clinical and medical affairs support for biotech and pharma teams — from protocol design and KOL engagement to publication strategy and regulatory interactions. Grounded in Nordic and EU practice, with an Oxford research background.
Medical affairs needs change by phase — I work project-by-project or as ongoing embedded support, joining wherever the current gap is.
Working alongside your team from the earliest stages to shape study design, endpoints, and overall medical strategy so the programme starts on solid footing.
Leading KOL engagement, advisory boards, and scientific communications as the programme moves toward pivotal data.
Supporting submission-ready documentation, medical writing, and publication planning as results mature.
Continued medical affairs input after launch — HCP education, real-world evidence generation, and lifecycle planning.
Engagements are scoped individually — a single deliverable, an interim role, or ongoing advisory support.
Study design, endpoints, and feasibility input from day one.
Ongoing clinical review and safety oversight during trials.
Identifying and coordinating key opinion leaders and panels.
Manuscripts, abstracts, and scientific communications.
Medical input into submissions and agency interactions.
Senior medical affairs capacity, without a full-time hire.
Reach out directly, or use the form — every message is emailed to me directly and I reply within two business days.