Mirriam Limage-Pierre

With over 15 years of extensive clinical-trial experience, Mirriam has extensive working knowledge of data management and GCP and ICH guidelines. As such, I oversee the activities of direct reports and serve as a mentor. I am also responsible for creating the CRF design and ensuring that all protocol required assessments are being collected and the database is built according to specifications. Specialities include; mentoring, leadership and coaching skills, matrix organization, project management skills, GCP/ICH guidelines, CRF Design, DB development, tables and listings, validations, derivations, database testing, SAE reconciliation, discrepancy management