Romain Paro
Coordinateur d'études, a suivre
Romain E. Paro, PhD
8’ rue Lisbonne, 75008 Paris
(+33) 607605460
8.romain@gmail.com
Summary of Qualifications: Wide-ranging knowledge in varied pharmaceutical and medical settings. Proven managerial capabilities. Demonstrated abilities to work effectively in a team. Highly experienced with European pharmaceutical industries, culturally sensitive. Skilled with personal computers. Research experience in pricing. Extensive travel experience and broad cultural awareness. Proficient in written and spoken English.
Objective: To obtain employment in a dynamic, international environment as a Health economic employee
6 contacts
2009 - 2010Worked in the corporate drug safety department of an international laboratory. Responsible of the preparation of all the safety reports to the Health Authorities (Periodic Safety Update Reports, Annual Safety Reports, FDA Report). Managed the international cases reported with medical analysis in the causality (French method of Imputability), the seriousness, and the listedness until the ICSR sent. Reconciliation of safety database and clinical database. Designed request for specific safety concerns.
2008 - 2009Worked in the French affiliate group as the French responsible of the pharmacovigilance. Reported all safety concerns to the corporate. Trained the new employee in pharmacovigilance.
2007 - 2008Worked in the medical management division of a lobbying, public affairs, and strategic advisory office. Served as a liaison between ADC and its affiliated laboratories. Represented ADC in meetings with customers. Developed a method in analysis of scientific literature that improved in-office efficiency. Active member of the Health and Eco-Strategy Consulting Cabinet as a writer of the Pricing and reimbursement files.
2006 - 2007Managed scientific committees composed of physicians and experts in the cardiovascular and respiratory fields. Conducted pharmacoepidemiological and pharmaceuticoeconomics studies in the cardiovascular and respiratory fields while working in the Health Outcome Studies Section (EES) of the Economic and Governmental Affairs Department. Successfully achieved a study protocol answering to the French Economic Committee on Drugs (CEPS). Monitored the positioning of cardiovascular and respiratory pharmaceutical-epidemiologic studies.
Pharmaco-epidemiology officer, Agence Française de Sécurité Sanitaire des Produits de Santé (AFSSAPS)
2005 - 2006Independently conducted investigation targeting thirty Risk Management Plans (RMP) while working for the National Department of Risk Monitoring, Ethical Use of and Information on Drugs (SURBUM). Produced pharmacovigilance reports for the EMEA working party. Served as the liaison between two French Public Authorities for post-launch drugs studies.
2005 - 2005Worked in the pharmacoepidemiology unit. Managed a research study on the economic incidence of gastro-intestinal side effects of the use of NSAIDs. Successfully improved my English communication.