• Prepare study documents for Ethics committee review and approval.
• Schedule the on-site visits with the Sponsor.
• Perform study socialization and conduct subject recruitment strategy.
• Implement subjects recruitment and screening.
• Schedule subject visit and coordinate study activities with field team, laboratory, and all related study personnel.
• Oversee the storage and accountability of Investigational Product.
• Maintain accurate and complete records.
• Close the study and archive the study records.

• Demonstrated ability to communicate in written and spoken English; is preferred
• Good interpersonal and communication skills.
• Good understanding and knowledge of Good Clinical Practice (GCP) and experiences in clinical trials is preferred.
• Open to work in a team work & individual; to organize a team or a group of trials participants.
• Responsive, creative, and adaptable to manage changes and solving problems.

[BEWARE OF RECRUITMENT SCAMS]

It has come to our attention that there are fake job offers claiming to be hiring for Siloam Hospitals Group. Please note that Siloam Hospitals Group do not require applicants to make payment when seeking employment with our hospitals.