Clinical Trial Coordinator
Atika joined EOCRU since July 2020. She started her career in clinical research as Data Management & Report Officer in 2008 and Clinical Research Associate in 2009 at Equilab International.
She continues her career as Clinical Research Associate in Quintiles (now IQVIA) since 2010. She has been Clinical Research Associate since 2009 until 2020. She was a Senior Clinical Research Associate. She has more than 10 years experience in clinical research industry, both in multinational pharmaceutical companies and Contract Research Organization (CRO). She has been involved for bioequivalence studies, experienced conducted pharmacokinetics analysis. She is experiencing to conduct clinical trial management including feasibility, start up, regulatory activities, initiation, monitoring, and closing from clinical trial phase II to phase IV, including observational studies.
She has been assigned as Indonesia representative to manage clinical trial system (CTMS) at IQVIA. She has been an co-author to publish two journals during her role as data management & report officer of bioequivalence study. The journal is in bioequivalence studies area.
Currently, Atika is working as study coordinator for COPCOV study, a prophylaxis study of Chloroquine to prevent COVID-19 in health-care settings.