Job Description

• To assist Chief Scientific Officer to monitor the administration and progress of a clinical trial to ensure timely delivery of key study milestones

• Oversees overall clinical trial operations related to the conduct of the clinical trial

• Provide clinical trial support including, but not limited to activities including site visit (overseas), meeting with Principal Investigators (PI), and monitor clinical trial process and understand the problems encountered

• Discuss progress and raise any red flags proactively with Principal Investigator and Chief Scientific Officer to ensure clinical trials follow and complete within timeline given

• Work with local clinical research organisation team to collect and ensure data completeness, consistency, and fulfil all regulatory requirements

• Work with local clinical research organisation team to prepare and summarize data required for submission to regulatory agencies (FDA & EMA etc)

• Work with Principal Investigator and Chief Scientific Officer to analyse data and prepare abstracts and manuscripts for publication in peer reviewed journals

• Work with software development team to validate algorithm and prepare publications
  

• Possess a PhD in clinical research related area

• Minimum 2 years of experiences in clinical research environments

• Publication (as first author) in clinical research related journals

• Ability to work both independently and in a team

• Good communication skills

• Meticulous and possess excellent organizational skills

• Willing to travel