Experience

Debiopharm

• Switzerland
• Pharmaceutical Manufacturing
• 300 - 400 Employee

• Clinical Trial Associate

  • May 2015 - Present

  Lausanne



IQVIA

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Senior Clinical Research Associate, acting as Clinical Research Specialist

  • Feb 2013 - Dec 2014

  St-Prex Key Responsibilities: - Act as subject matter expert for operational conduct of the assigned protocol(s) at site and ensure that clinical monitoring tasks are conducted in accordance with protocol, process, quality standards and expectations, per Contract. - Oversee the work of assigned CRAs, providing advice and guidance to help achieve quality deliverables on site. - Coordinate sites until study closure, including start-up activities and assistance with IRB/EC submission process… Show more Key Responsibilities: - Act as subject matter expert for operational conduct of the assigned protocol(s) at site and ensure that clinical monitoring tasks are conducted in accordance with protocol, process, quality standards and expectations, per Contract. - Oversee the work of assigned CRAs, providing advice and guidance to help achieve quality deliverables on site. - Coordinate sites until study closure, including start-up activities and assistance with IRB/EC submission process (both central and local submissions), covering all countries for the selected study - Review protocol and assist with case report form design, and develop study monitoring plans for assigned studies

• Clinical Project Coordinator

  • Sep 2011 - Feb 2013

  St-Prex Key Responsibilities: - Participate in internal / client project meetings and take minutes as integral member of the project management team. - Manage timelines, assist with budget tracking and responsible for coordinating vendor activities including cost proposals and service requests - Develop and maintain, based on project scope, project tracker from completion of site selection to study close-out and study master file - Contribute to development and distribution of site… Show more Key Responsibilities: - Participate in internal / client project meetings and take minutes as integral member of the project management team. - Manage timelines, assist with budget tracking and responsible for coordinating vendor activities including cost proposals and service requests - Develop and maintain, based on project scope, project tracker from completion of site selection to study close-out and study master file - Contribute to development and distribution of site communications including newsletters, webinars.



Pharmacie Miserez

• Pharmacist

  • Oct 2010 - 2011

  Bussigny-près-Lausanne - Responsible for dispensing medication and ensure correct use of drugs/medical devices and identify and report Adverse Drug Reactions and Adverse Events. - Provide information and advice on health, and monitor upon request patient health (BP, glycaemia, cholesterolemia) - Ensure identity and purity of herbal drugs and chemicals used or delivered. - Prepare extemporaneous medical preparations, order and manage stocks and turn-over of goods. - Manage team members.



University of Geneva

• Switzerland
• Research Services
• 700 & Above Employee

• PhD Student and Teaching Assistant

  • Mar 2006 - Sep 2010

  PhD student under the supervision of both Prof. Pierre-Alain Carrupt (head of the Pharmacochemsitry lab, UniGe) and Prof. Hugues Abriel (head of the Ion Channels lab, UniBe) Key Responsibilities: - Create teaching material for Master courses. - Prepare and supervise practical works of Bachelor/Master students in the Section of Pharmaceutical Sciences



Several pharmacies

• Pharmacist

  • 2003 - 2009

  Regular or punctual work as a pharmacist in several pharmacies in Lausanne and surroundings.