Maren Roller

CRF / eCRF Data Entry and Query Solution, Review Informed Consent Forms according to ICH-GCP, Assure Quality of CRF Data, Source Data and Clinbase Data entries

Assisting on study specific projects, generating MSP timelines, client and monitor communication, TMF and ISF maintenance, assisting on the management and set up of early phase clinical trials in consideration of proposed timelines and GCP guidelines, preparing and overseeing monitoring visits, assisting the Project Manager with monitoring and managing the study budget and ensuring all milestones are met, set up and regular review of the Study Files

physiology, anatomy, pathology, english, biochemistry, clinical monitoring, bioethics, principles of Drug actions, biostatistics, guidlines and laws, data management, drug development, pharmacology, work placement (5th semester), project management