Working under the contract with Sanofi (as Clinical Project Leader, Local study manager)Responsibilities:- Responsible and accountable for the management of the Clinical Operations team- Develop the strategy, plans, tools and training to oversee and assess the performance of the clinical team- Ensure that all study clinical related documents are tracked. filed and reviewed- Responsible and accountable for understanding and managing the clinical operations budget-… Show more Working under the contract with Sanofi (as Clinical Project Leader, Local study manager)Responsibilities:- Responsible and accountable for the management of the Clinical Operations team- Develop the strategy, plans, tools and training to oversee and assess the performance of the clinical team- Ensure that all study clinical related documents are tracked. filed and reviewed- Responsible and accountable for understanding and managing the clinical operations budget- Communicate effectively and proactively with all members of the project team Show less

Working under the contract with Sanofi

Working under the contract with SanofiResponsibilites:Responsibilities:- Responsible and accountable for the site monitoring management- Responsible for clinical studies according to Company, and/or Sponsor Standart Operating Procedures, and local regulatory guidelines- Assures the implementation of project plans, as assigned- Act in the project role of a Local Project Coordinator or Lead CRA as assigned

- Monitored protocols (phase III and IV) within Cardiology, Rheumatology, Dermatology, Otolaryngology and Oncology at multiple sites across the country.- Conducted site initiation, interim, and closeout monitoring visits to confirm compliance with the protocol and adherence to ICH-GCP.- Perform and coordinate all clinical monitoring and site management process for assigned projects in accordance with GCP, FDA, local regulations and sponsor‘s SOPs.- Ensure timely submission and… Show more - Monitored protocols (phase III and IV) within Cardiology, Rheumatology, Dermatology, Otolaryngology and Oncology at multiple sites across the country.- Conducted site initiation, interim, and closeout monitoring visits to confirm compliance with the protocol and adherence to ICH-GCP.- Perform and coordinate all clinical monitoring and site management process for assigned projects in accordance with GCP, FDA, local regulations and sponsor‘s SOPs.- Ensure timely submission and review of CRF data and query resolution according to required timelines- Build and maintain relationship with Investigator and site staff to assure an effective collaboration- Maintain required documentation in the Investigator Site File and provide required documentation from site for the Trial Master File according to SOPs.As an employee of CRO I was assigned to:July 2016 – February 2017: AmgenSince February 2017: Sanofi Show less

Sales Representative – actively working in the pharmaceutical market pushing the company’s products

Training program

direct contact with customers (B2C), dealing with customer, customer problem solving