La Rippe, Vaud, Switzerland
With my skills to manage end-to-end projects, creating alliances with internal and external stakeholders to develop and execute strategic plans, combined with my experience and business acumen, I develop leadership, accountability and responsibility in others with the vision of shaping an engaged and high performing work environment in order to meet and satisfy client expectations
Provides strategic and operational leadership of clinical research studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs. Independently leads complex, large, global in-house or outsourced, Non-Registrational Data Generating or Registrational Data Generating trials/studies at any point in the life cycle of the trial/study (i.e. start up, maintenance, or close-out). Acts as the primary operational contact for the study and leads the cross functional global team for execution of the study. May provide operational leadership of one or more cross-functional Study Team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO) teams and vendors. Has high global organizational impact and influence, and significant impact on function and Study Team
Provides strategic and operational leadership of clinical research studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs. Independently leads complex, large, global in-house or outsourced, Non-Registrational Data Generating or Registrational Data Generating trials/studies at any point in the life cycle of the trial/study (i.e. start up, maintenance, or close-out). Acts as the primary operational contact for the study and leads the cross functional global team for execution of the study. May provide operational leadership of one or more cross-functional Study Team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO) teams and vendors. Has high global organizational impact and influence, and significant impact on function and Study Team.
Leads successful and timely operational execution of global insourced or outsourced, Non-Registrational Data Generating or Registrational Data Generating interventional clinical trials from concept to final clinical study report. Acts as the primary operational contact for the study and leads the cross-functional global team for execution of the study. May provide quality oversight of one or more Contract Research Organization (CRO) teams and vendors. Focuses on project management concepts to support management of issues, risks, timelines, and budget and ensures quality compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs.
In addition to the below listed responsibilities, managing a client relationship on a global account level with the goal to attract new business opportunities for the organization Introducing and overseeing process improvement initiatives to strengthen the relationship between the client and Covance Primary point of contact for all client/study related issues on an account level
Knowledgeable and experienced in project management techniques related to clinical trials. Responsible and accountable for key client deliverables including budget, risk and milestone management. Combining a strong understanding of client protocol specifies and study feasibility to ensure successful study management and provision of outstanding customer service. Liaison between clients, CRO and Covance and displaying strong leadership to ensure successful interactions between Covance study team members. Manages a portfolio of global and high complexity studies.
Responsible for day to day coordination and supervision to ensure the successful implementation of the global site support strategy, structures, processes and metrics in order to deliver outstanding customer satisfaction