To conduct and oversee the implementation of clinical research and trials on cognitive impairment according to study protocol, SG-GCP, hospital policies, and applicable regulatory and ethics requirements.

Roles and Responsibilities

• Compliance with the SGGCP and other applicable regulatory and ethical requirements as well as hospital policies if applicable.
• Assist the Principal Investigator in applying to the NHG Domain Specific Review Board (DSRB) or Institutional Review Board (IRB) for ethics review and to the Health Sciences Authority (HSA) for clinical trial certificates (if required)
• Coordinate and manage all aspects of clinical research and trials from site initiation, subject recruitment, data collection, to study close-out.
• Identify, recruit, and screen potential study subjects based on protocol criteria.
• Administer informed consent to enrolled subjects.
• Schedule study visits and procedures, pr...