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This is a strategic global feasibility role within the European headquarters of a leading biotech company! In this job you will lead and co-ordinate feasibility assessments at the program, protocol and site level to support clinical development teams with study placement decisions. Working closely with operations staff and external vendors you will plan all feasibility activities, allocating resource where necessary and ensuring that all assessments are delivered to key stakeholders within set timelines. Youll have ownership of the feasibility process, contributing to the improvement and efficiency of this process on a global level, and assessing the effectiveness of new novel technologies and data sources on improving the way in which feasibility is conducted by the company. Based from the companys office in East Anglia or Middlesex you can expect to travel globally up to 15% of the time. Who should apply? We are looking for candidates with broad experience in biopharmaceutical R&D with time spent working in a CRA or project manager role. You will have a strong understanding of the drug development process and project management tools and processes. You will be comfortable presenting project data to senior management and have strong customer service skills. More importantly you will be able to demonstrate the skills required to work independently across departments within a matrix environment. This is a great opportunity to move into a strategic role within an expanding and high profile department!