About this role
Contract Type: 1-year contract
Roles & Responsibilities
You will be required to oversee research studies and related research and administrative activities such as:
- Pre-study preparatory activities
- Study recruitment and coordinate other research related activities such as study monitoring, maintaining participant logs
- Coordinate with other study sites and collaborating with institutes
- Organise and coordinate workflow of studies and assist with subject informed consent process
- Prepare study applications, reports, and documentations
Requirements
- Bachelor’s degree in sciences, Public Health or equivalent
- Experience in clinical research would be advantageous
- Good written communication skills
- Able to work independently and resourceful
- Relevant training will be provided when necessary