Roles and Responsibilities
Freshers are eligible to apply.
Conduct clinical trials, ensuring compliance with ICH-GCP guidelines.
Manage clinical data using CDM systems, adhering to regulatory requirements.
Collaborate with cross-functional teams for drug safety assessment and pharmacovigilance activities.
Ensure timely submission of reports and documents related to clinical operations.
Maintain accurate records of study protocols, case report forms (CRFs), and other relevant documentation.