2012 - 2013* Filing: Maintain study files, perform regular documented review and reconciliation, ensure updating of centre’s files and general files, handle all logistical aspects of a clinical trial
* Site Management: Manage relationship with sites, Follow-up studies by phone: administrative management of sites and patients, Administrative management of investigators contracts, Assist in the coordination between the local depots, local couriers and sites, provide support to sites
* Co-Monitoring: Participate on initiation visits of Oncology study Phase II and co-monitoring visits of diabetic study phase III, Oncology study Phase II and Relapsing Multiple Sclerosis Phase III
* Regulatory: Collect regulatory and administrative documents for the creation and submission of regulatory dossier to EC and MoH, prepare Import License application
* Payment: Issue invoices for investigators
* Audit: Participate to site investigators audits and system audits
* Tracking: Completion of study trackers
* Investigational Medical Product: Accountability of IMP, dealing with customs broker, follow on IP accountability, return & destruction
* Feasibility: Selection of investigators, data and essential documents collection: Phase III Hepatocellular Carcinoma study and Natural History study
