Clinical Trial Administrator

Role Overview Novo Nordisk India is looking for a dedicated Clinical Trial Administrator to join its CDC India team based in Bengaluru. This role involves providing end-to-end administrative and operational support for clinical trials conducted by Novo Nordisk India, ensuring all activities are carried out in compliance with GCP guidelines and applicable local regulatory requirements. The position reports directly to the Manager, Clinical Operations and plays a key role in facilitating timely and high-quality clinical project deliverables. Key Responsibilities - Provide support to Trial Managers and Clinical Research Associates across all phases of clinical trial activities including start-up, execution, and closure - Handle customisation and translation of study documents as required - Manage Health Authority and Ethics Committee submissions in line with regulatory standards - Oversee contracts, auxiliary supplies, and trial product management - Support the organisation of global and local investigator meetings and departmental events - Process study payments and maintain accurate electronic and physical filing of study documents - Ensure all activities comply with ICH-GCP guidelines, local regulations, and Novo Nordisk standard operating procedures Required Qualifications - Graduate degree in Science, Pharmacy, or Medicine; additional qualification in Clinical Research is preferred - Minimum 1 year of experience in clinical research or a similar role such as CRC or CTA - Trained in ICH-GCP guidelines; certification is an added advantage - Strong written and verbal communication skills with keen attention to detail - Ability to work both independently and collaboratively within a team environment - Demonstrated capability to plan, execute, and follow up on trial-related tasks Why Join Us At Novo Nordisk, you will be part of a global organisation with over a century of commitment to defeating serious chronic diseases and improving patient lives. This is an opportunity to grow alongside exceptional professionals while contributing to meaningful healthcare innovations that make a lasting difference.

- Graduate in Science, Pharmacy, or Medicine - Minimum 1 year experience in clinical research or CRC/CTA role - Training in ICH-GCP guidelines; certification preferred - Strong written and verbal communication skills - Attention to detail and ability to manage multiple tasks - Experience with Health Authority and Ethics Committee submissions - Ability to work independently and as part of a team - Familiarity with study document management and electronic filing systems

- Opportunity to work with a globally renowned pharmaceutical organisation - Professional and personal development opportunities - Inclusive and diverse work environment - Exposure to international clinical trial standards and processes