Clinical Research Coordinator
QuartesianClinicalResearchPvt
Hyderabad
·3 w
·Full time
·Healthcare
$400,000 Per Year
$1,200,000 Per Year
Coordinates the conduct of clinical trials at the site level. Manages patient recruitment, screening, and enrolment processes. Obtains informed consent and ensures ethical compliance in trials. Maintains accurate case report forms and study documentation. Coordinates investigator meetings and site initiation visits. Manages study drug accountability, dispensing, and reconciliation. Schedules and coordinates study visits with participants and teams. Liaises with sponsors, CROs, and ethics committees. Ensures GCP and ICH guidelines compliance throughout trial conduct. Handles adverse event reporting and safety notifications. Manages site master file and essential document maintenance. Prepares site for monitoring visits and audits by sponsors. Trains site staff on study protocols and regulatory requirements.