Responsibilities: Communicate and collaborate on global study activities working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines and Coordinate project meetings and produce quality minutes. Qualifications: PhD in Life Sciences Research experience must be related to Cardiovascular or Metabolic such us diabetes, metabolicsyndrome, hyperlipidemia etc. Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry
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