TJ Pharma Consulting

Providing strategic advice and hands-on support for biotech and Pharma companies with the regulatory, commercial and market access endgame in mind, based on a track record of succesful planning and execution of multiple clinical development plans from Ph1 up to multiple regulatory submissions to FDA, EMA and RoW. Further areas of proven expertise are indication sequencing, clinical trial design and conduct, safety management, data analyses, resource planning, leading health authority meetings, advisory boards or scientific interaction and publications in a variety of therapeutic areas, including but not limited to rare disease, pediatrics, hepatology/gastrointestinal, cardiovascular and neuroscience. Having built and led the European hub of an US biotech, I can help biotech companies establish their oversea office and build their European team and support network.