Ensure that projects are delivered on time, within budget, and agreed scope, maintaining the appropriate industry, sponsor and Ergomed quality standards Liaise with project team members, provide training where needed and ensure correct allocation to tasks Develop, review and edit project plans to assure consistency with goals and milestones Organization and facilitation of project meetings related to study activities (study organization, initiation, execution, closure) Serve as primary point of contact with sponsor and Ergomed Senior Management on project status Represent Ergomed at external meetings, providing liaison with scientific/medical experts in other CRO/Sponsor companies and for committee meetings, (e.g.EC/IRB) Develop review and edit of relevant SOPs to assure consistency with Regulatory standards and develop study related training programs to support this. Contribute to bid defense activities 
