Job Description

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

Skills Required