Novo Nordisk Hiring Clinical Trial Administrator role
- Novo Nordisk Hiring Clinical Trial Administrator in Bangalore | Pharma Clinical Research Jobs 2026
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Qualification:
- Relevant Courses:
- Experience:
- Skills Required:
- Location & Salary
- Job Location:
- Salary:
- Application Process
- Important Deadline:
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What is the required qualification?
- 3. Is GCP certification mandatory?
- 4. What is the job location?
- 5. What type of role is this?
- Summary
Novo Nordisk Hiring Clinical Trial Administrator in Bangalore | Pharma Clinical Research Jobs 2026
Novo Nordisk India Pvt Ltd is hiring for the position of Clinical Trial Administrator (CTA) under the Clinical Development department in Bangalore. This opportunity is ideal for candidates with a background in life sciences, pharmacy, or medicine who are looking to build a strong career in clinical research and clinical trials management.
This hiring is for 1 vacancy in the Clinical Operations team, and candidates with at least 1 year of experience in clinical research roles such as Clinical Research Coordinator (CRC) or CTA are eligible to apply. The job location is Bangalore, Karnataka, one of India’s leading hubs for pharmaceutical and biotech companies.
Company Overview
Novo Nordisk is a globally recognized healthcare company headquartered in Denmark with over 100 years of excellence in pharmaceutical innovation. It is a leader in diabetes care and is expanding its footprint across multiple therapeutic areas including obesity, rare diseases, and chronic conditions.
With more than 63,000 employees worldwide and a strong presence in India, Novo Nordisk is known for high-quality clinical trials, regulatory compliance, and patient-centric healthcare solutions. The Bangalore affiliate office houses over 1,300 professionals working across clinical research, regulatory affairs, pharmacovigilance, and data management.
Working at Novo Nordisk offers exposure to global clinical trial operations, advanced research systems, and a culture focused on innovation, compliance, and patient safety.
Job Role & Responsibilities
As a Clinical Trial Administrator, you will play a key role in supporting clinical trial operations and ensuring smooth execution of clinical research projects.
Key Responsibilities:
- Support clinical trial start-up, execution, and close-out activities across India
- Prepare and manage essential study documents and regulatory submissions
- Coordinate submissions to Health Authorities and Ethics Committees
- Assist in site set-up, contract management, and investigator coordination
- Manage clinical trial supplies, logistics, and inventory tracking
- Support investigator meetings and internal clinical team coordination
- Maintain accurate trial documentation in electronic systems (eTMF, CTMS)
- Assist with study payments and financial tracking
- Ensure compliance with ICH-GCP guidelines and regulatory requirements
This role is critical in maintaining clinical trial quality, regulatory compliance, and timely delivery of study milestones.
Eligibility / Qualifications
Educational Qualification:
Candidates must have a degree in one of the following:
- B.Pharm, M.Pharm, Pharm.D
- B.Sc / M.Sc Life Sciences
- MBBS or Medical degree
- Clinical Research certification (preferred)
Relevant Courses:
B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Clinical Research, Biotechnology, Microbiology, Biochemistry, MBBS, Clinical Data Management, Regulatory Affairs
Experience:
- Minimum 1 year experience in clinical research
- Experience as Clinical Research Coordinator (CRC), CTA, or similar roles
- Knowledge of ICH-GCP guidelines is preferred
Skills Required:
- Strong communication and documentation skills
- Attention to detail and regulatory compliance understanding
- Ability to manage multiple clinical projects and timelines
- Team collaboration and independent working capability
Location & Salary
Job Location:
- Bangalore, Karnataka (On-site role)
Salary:
- Not disclosed (Competitive industry-standard package with benefits)
Employees benefit from strong career growth, exposure to global trials, and a structured clinical research environment.
Application Process
Interested candidates can apply through the official Novo Nordisk careers portal:
Apply Here: https://careers.novonordisk.com/job/Bangalore-Clinical-Trial-Administrator-Karn/1376745833/
Important Deadline:
- Last Date to Apply: 27 March 2026
Candidates are advised to apply early to secure their opportunity in this high-demand clinical research role.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
No, at least 1 year of clinical research experience is required.
2. What is the required qualification?
Candidates with pharmacy, life sciences, or medical degrees can apply.
3. Is GCP certification mandatory?
It is preferred but not mandatory.
4. What is the job location?
Bangalore, Karnataka.
5. What type of role is this?
Full-time clinical research role in clinical operations.
Summary
| Category | Details |
|---|---|
| Company | Novo Nordisk |
| Vacancies | Clinical Trial Administrator |
| Required Education | B.Pharm, M.Pharm, B.Sc, MBBS |
| Experience | Minimum 1 Year |
To apply for this job please visit careers.novonordisk.com.
