Must have valuable knowledge of ICH-GCP, New Drugs and Clinical Trials rule 2019, able to coordinate with principal investigator and sponsor for startup activities of trial projects, patient's screening, randomization, source documentation, site master file maintenance, eCRF entry, sample collection, storage, lab report collection, reporting & follow up SAEs, Ethics committee coordination, study doc archiving. able to prepare EC notification and submissions. Minimum 6 months experience required.
Freshers are eligible, if enthusiastic and willing to learn.