Carries out assigned administrative duties to support clinical trial conduct
Sets up Investigator Site File, according to SOPs provided either by the Sponsor or by ERGOMED, and distribute to sites
Coordinates and attends project meetings (e.g. investigator, kick-off, team, etc.) with the PM/CTM. Supports preparation of meeting agenda and provides written high-quality meeting minutes within specified timeframe
Works with project teams to assist in tracking, naming and routing of clinical trial documentation to the Trial Master File (TMF)
Maintains contact lists, information for project team members (e.g. project training records) and other trackers as required. Provides reports from tracking tools.
If requested attends in-house audits and supports completion of Corrective and Preventative Action Plan
Any other task related to the specific clinical trial performance