If you are looking to build a strong career in clinical research and clinical trial operations, this opportunity at Novo Nordisk India Pvt Ltd is highly valuable. The company is hiring for a Clinical Trial Administrator (CTA) role in Bangalore, offering exposure to global clinical trials, regulatory processes, and end-to-end study management.

This Clinical Trial Administrator job in Bangalore is ideal for candidates with 1+ year experience in clinical research, CRC, or CTA roles, and those who want to grow in clinical operations, trial management, and regulatory compliance.

Key Responsibilities – Clinical Trial Administrator (CTA)

• Support clinical trial start-up, execution, and close-out activities
• Prepare, customize, and manage study document translations
• Coordinate Ethics Committee and Health Authority submissions
• Assist in site set-up and contract management
• Manage clinical trial supplies and logistics
• Provide administrative support for investigator meetings
• Handle study payments and documentation (eTMF & physical files)
• Maintain clinical trial trackers and systems
• Ensure compliance with ICH-GCP guidelines and regulatory requirements

Qualifications & Eligibility Criteria

• Graduate in B.Pharm / M.Pharm / Life Sciences / Medicine
• Minimum 1 year experience in Clinical Research (CTA/CRC roles)
• Knowledge of ICH-GCP guidelines (GCP certification preferred)
• Strong communication and documentation skills
• Good understanding of clinical trial processes and regulatory workflows
• Ability to manage multiple tasks and work in a team environment

Why Join Novo Nordisk? (Benefits & Career Growth)

• Work with a top global pharmaceutical company
• Exposure to international clinical trials and regulatory submissions
• Opportunity to grow in Clinical Operations / CRA / Project Management roles
• Strong learning environment with structured processes
• Contribute to healthcare impacting 40+ million patients globally

Application Process

Application Link