Job Description

Clinical Trial Administrator

Department – CDC India

Organization – Novo Nordisk India Pvt Ltd (Affiliate)

Job Level – 5

Are you experienced Clinical research professional and passionate about clinical trials? Does being part of a growing, yet dynamic environment excite you? If yes, then you may be the one we are looking as Clinical Trial Administrator (CTA) for Novo Nordisk India, Bangalore.

About the company
Novo Nordisk is a Denmark based multinational with leadership in diabetes. Novo Nordisk India affiliate office is located in Bangalore & has more than 1700 people working across the country in various functions. The CTA position reports directly to the Manager, Clinical Operations.

The position
As a CTA, you will provide support to the CDC Trial Managers and CRAs in relevant aspects of trial activities in CDC-India (start-up, execution and closure) and facilitate timely clinical project deliverables of required quality by Novo Nordisk India in accordance with Good Clinical Practice (GCP) guidelines and in line with local regulatory requirements.

The scope of CTA activities for a particular clinical trial may vary with respect to countries sponsored. The activities start post country allocation and ends after study documents are sent for central archival post completion of trial.

In this role your main responsibilities will be customization and translations of study documents, Health Authority and Ethics Committee submissions, contracts, auxiliary and trial product supplies management, support for arranging global/local investigator meeting and other departmental meeting or related activities, study payments, systems, filing of study documents (electronic and physical copies) and any tasks assigned as per project needs in compliance with local regulations, ICH-GCP, Novo Nordisk procedures and protocol requirements.

Qualifications

Below are the required skills.

• Graduate in Science, Pharmacy or Medical. Additional Qualification in Clinical Research would be preferred.
• At least 1 year of experience in Clinical Research or in similar job profile such as CRC/CTA.

• You are required to be trained in ICH-GCP guidelines and if applicable certification is also preferred.

• Should have very good communication skills (both written and verbal), able to work efficiently with team and as individual, eagerness to learn and attention to detail.
• Demonstrated ability to plan, execute and follow-up of trial related activities (applicable for this position).

Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. You share the same passion and commitment as our employees in our journey to make a difference to patients’ lives. In exchange, we offer you the chance of a lifetime to work with extraordinary talent and benefit from unmatched opportunities for professional and personal development.

Deadline: 23 June 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.