Responsibilities
To support Project related to research
Take consent from research participants before performing any research procedures
Proper handling and preservation of subject of studies
Perform data entry and data QC of data forms and reports
Maintain clinical inventory and equipment
Train and assess staff in performing health s...
To coordinate and assist in the conduct of clinical research studies and trials in compliance with study protocols, applicable laws and regulations, principles, guidelines, policies and procedures.
For interested candidates, please send your updated resume:
Responsibilities
You will assist the principal investigator to develop and implementation:
To prepare documents for and facilitate regulatory Approvals
To facilitate the signing of project agreements with external collaborators.
To implement and monitor programme activities and workflow.
To facilitate programme-related outreach events an...
Responsibilities:
Responsible to handle patients in basic treatments
Educate patients on the disease progress
Encourage self-management
Identify at-risk patients
Perform some outcome management and tracking of data.
Perform office hours duties
5 days (5 half days / 3 full days / Part Time)
Nursing admin positions available too (off...