Company Name: Dexa Group
Location: Jakarta Selatan
Posted Date: 08/10/2024 16:51
Salary:
Job Description
Job Description:
- Prepare clinical study documents (protocol, CRF, Informed Consent Form, etc.)
- Assist Principal Investigator for Ethics Committee submission
- Responsible for Regulatory Affairs submission
- Perform site feasibility, investigator selection, and site set up
- Perform clinical trial monitoring, follow up and discussion with study site team
- Responsible for maintaining trial documentation
- Acting as a communication line between investigator and sponsor
Requirements:
- Bachelor’s degree from Pharmacy (preferably Apothecary graduates)
- At least 1 year experience as the CRA, Regulatory/Registration in Pharmaceutical Companies, Clinical Research Industry or Hospital
- English proficiency is preferred
- Open & flexible to travel