Medical Advisory

Strategic medical guidance throughout product development

Sponsors and CROs often need senior medical input without the overhead of a full-time Medical Director.

Independent advisory support helps bridge the gap between scientific ambition and operational feasibility — ensuring that study design, safety strategy, and communication with regulators and investigators are grounded in sound medical reasoning.

At CLT Vigilance Consulting, Medical Advisory provides experienced, independent medical guidance to support confident and well-informed decisions across the product life cycle.

Core activities include:

Providing medical input to study design, endpoints, and protocol development.
Advising on eligibility criteria and risk mitigation strategies.
Supporting Investigator Meetings, medical training, and communication with Key Opinion Leaders (KOLs).
Acting as a medical sounding board for operational teams and sponsor leadership.
Reviewing clinical documentation such as Investigator’s Brochure (IB), Clinical Trial Protocol (CTP), Clinical Study Report (CSR), and case narratives for medical accuracy.

Value to client

CLT Vigilance Consulting provides senior-level medical expertise, grounded in the experience of Cornelia Lif-Tiberg, MD, to support clarity, confidence, and credibility in clinical decision-making.

Combining clinical depth with a pragmatic understanding of operational realities, this approach enables sponsors and CROs to balance scientific ambition with feasibility, while maintaining the highest standards of medical, ethical, and regulatory integrity.

With experience across organizations of different sizes and maturity levels, CLT Vigilance Consulting is particularly well positioned to support start-ups and scale-ups in navigating complex development decisions.