Candidate with PhD, 10 years experience as senior CRA and Trial lead CRA, in CROs and pharmaceuticals, over 8 years experience in academic research as team coordinator.
Currently responsible for phase I insourced studies and for insourced and outsourced feasibilities for all studies in all therapeutic areas. Member of international working groups and task forces.
General skills: excellent presentation skills, field and time management, liaising with KOLs and SMEs, PIs and vendors (CROs included).
Monitoring and co-monitoring (all types of visits), site selection, training and mentoring to CRA juniors and internal and external staff, start-up activities and review of local WPs, protocols and ICFs, support to overview of outsourced studies (including co-monitoring visits and newsletters).
Main Therapeutic areas: hematology and oncology, phases I-II-III studies, orphan drugs.
Experience in biological drugs in rheumatology.
Also good experience gained in academic year in teaching genetics and experimental biology, planning in vivo and in vitro scientific experiments, writing papers, posters and grants, giving scientific presentations to international audiences, mentoring of PhD students