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
+ And/ or other study related task given by the PI
Qualification
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
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