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Clinical Trial Administrator
Actively Reviewing
Novo Nordisk
Job Description
Department - CDC India
Organization : Novo Nordisk India Pvt Ltd
About us Novo Nordisk is a global healthcare company headquartered in Denmark and a leader in diabetes care. Novo Nordisk India’s affiliate office in Bangalore employs more than 1,300 people across diverse functions. We are committed to making a difference for patients through high-quality clinical research and development.
The role We are looking for a Clinical Trial Administrator (CTA) to join the Clinical Department and report to the Manager, Clinical Operations. In this role you will support CDC Trial Managers and CRAs across trial start‑up, execution and closure activities in India. You will help ensure timely delivery of clinical project activities in compliance with ICH‑GCP, applicable local regulations and Novo Nordisk procedures.
Key responsibilities
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing.
Contact
To submit your application, please upload your CV online (click on Apply and follow the instructions).
Deadline
27th March 2026.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
Organization : Novo Nordisk India Pvt Ltd
About us Novo Nordisk is a global healthcare company headquartered in Denmark and a leader in diabetes care. Novo Nordisk India’s affiliate office in Bangalore employs more than 1,300 people across diverse functions. We are committed to making a difference for patients through high-quality clinical research and development.
The role We are looking for a Clinical Trial Administrator (CTA) to join the Clinical Department and report to the Manager, Clinical Operations. In this role you will support CDC Trial Managers and CRAs across trial start‑up, execution and closure activities in India. You will help ensure timely delivery of clinical project activities in compliance with ICH‑GCP, applicable local regulations and Novo Nordisk procedures.
Key responsibilities
- Support start‑up, execution and close‑out activities for assigned clinical trials in India.
- Prepare, customize and coordinate translations of study documents.
- Manage submissions to Health Authorities and Ethics Committees.
- Support contract administration and site set‑up activities.
- Coordinate auxiliary and trial product supplies and inventory.
- Provide logistics and administrative support for investigator meetings and other departmental meetings.
- Support study payment processing and study documentation filing (electronic and physical).
- Maintain trial-related systems and trackers.
- Perform other project‑related tasks as assigned to meet regulatory and quality requirements.
- Graduate in Science, Pharmacy or Medicine. Additional qualification in Clinical Research is desirable.
- Minimum 1 year of relevant experience in clinical research or similar role (e.g., CRC, CTA).
- Trained in ICH‑GCP; GCP certification is preferred if available.
- Strong written and verbal communication skills.
- Excellent attention to detail, ability to work both independently and in a team, and a strong willingness to learn.
- Proven ability to plan, execute and follow up trial‑related activities.
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing.
Contact
To submit your application, please upload your CV online (click on Apply and follow the instructions).
Deadline
27th March 2026.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
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