The Indonesia Research Partnership on Infectious Disease (INA-RESPOND) is a collaborative initiative between United States and Indonesian government institutions formed to promote and conduct high-quality infectious disease clinical research in Indonesia through development of a collaborative, sustainable, and well-recognized research network.- Site selection, study start up, site initiation, study management and study close out- study site operational and management- study budgeting and supplies management- Involved in HIV observational study and clinical trial, psychiatry observational study on HIV, and COVID-19 observational study and clinical trial - Material Transfer Agreement preparation and submission for COVID-19 study

- study feasibility- study start up for asthma study and oncology study

- Site monitoring visit on dengue vaccine study

- Site selection, study start up, site initiation, site monitoring and site close out visit- Involved in formula milk study , food supplement study and oncology studies (colorectal cancer and hepatocellular cancer)- participated in NADFC inspection and sponsor audit

- Site selection, study start up, site initiation, site monitoring and site close out visit- Involved in formula milk study, food supplement study and oncology studies (colorectal cancer and hepatocellular cancer)- participated in NADFC inspection and sponsor audit

- Study feasibility, study start up, site initiation, and site Monitoring - Involved in asthma study and diabetes study

- Site selection, study start up, site initiation, site monitoring and site close out visit- involved in the development and maintain internal CRO SOP- contraceptive clinical trial, urology study, dermatology study, nutrition for pediatric study, and cardiology study- Material Transfer Agreement preparation and submission for dermatology study, - participated in NADFC inspection in contraceptive clinical trial

- Secretary to Medical Director- Maintain logistical aspect of clinical trial- Assisting CRA in the IRB/EC submission, regulatory submission- Manage site payment- Maintain study file and archiving study document- Arrange investigator meeting- Deputy study drug coordinator : maintain investigational product storage, shipment, accountability and distribution to study site