Job Descriptions:

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.

Requirements:

• 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.
• Willing to be placed in Cikarang Area (Accordingly to the projects availability).