Clinical Research Associate

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.