Accelerating Oncological Breakthroughs

Maud Jonnaert
Clinical Development Expert
Clinical development expert with 15 years of experience in the pharmaceutical industry. Passionate about advancing drug candidates from the pre-clinical stage to successful proof of concept.
Drive Your Early Clinical Development
Time matters in cancer treatment, let me support you in transforming your innovative scientific concept into a robust clinical development plan.

Clinical Development Plan

Designing investment conscious clinical development plans. Target population definition, design and review of patient-centric protocol, dose selection, drug combination optimization.

Clinical Study Preparation

Timeline optimization from IND/CTA to enrollment of the first patient. Protocol, Investigator Brochure and informed consent writing. eCRF design with an emphasis on clinically relevant data. Site and clinical research associate training.

Clinical Study Conduct, Data Integrity & Analysis

Optimizing interaction between all stakeholders. Monitoring, reviewing and summarizing safety and efficacy data in ongoing clinical studies. Development of clinical trial reports and publications.

Due Diligence

Interpretation of pre-clinical and clinical data to understand the value and risks of an early oncology asset from a clinical development perspective. Providing guidance for an early clinical development plan.

Together Against Cancer!

Clinical consulting focused on early phases for biotech to guide oncology clinical development.
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