Apply for Clinical Research Associate at Novo Nordisk Mumbai. Check eligibility, experience, responsibilities, salary details and apply before deadline now online.
Introduction
If you have experience in clinical trials and want to work with a globally reputed pharmaceutical company, this is a strong opportunity. The Clinical Research Associate at Novo Nordisk role focuses on site monitoring, patient safety, and ensuring high-quality clinical trial execution. This position is ideal for professionals aiming to grow in clinical operations and global research projects.
Job Overview
| Job Title | Clinical Research Associate (CRA) |
|---|---|
| Company Name | Novo Nordisk |
| Location | Mumbai (Primary), Bangalore (Department Base) |
| Employment Type | Full-Time |
| Department | Clinical Development (CDC India) |
| Experience Required | 2–4 Years |
| Education | Degree in Medicine / Pharmacy / Life Sciences |
| Salary | As per company standards |
Company Overview
Novo Nordisk is a leading global pharmaceutical company known for its innovation in diabetes care, obesity treatment, and chronic disease management. With over 100 years of experience, Novo Nordisk focuses on improving patient outcomes through research-driven healthcare solutions and advanced clinical development programs.
Job Location & Employment Type
- Primary Location: Mumbai, India
- Department Base: Bangalore, India
- Employment Type: Full-Time
- Travel: Flexible travel required
Open Positions / Department Details
This role is part of the Site Monitoring Excellence team within Clinical Development. The team ensures high-quality execution of clinical trials by managing sites, monitoring data, and maintaining compliance with regulatory standards.
Key Roles & Responsibilities
Site Management & Monitoring
- Act as the main contact between the company and clinical trial sites
- Conduct on-site and remote monitoring visits
- Ensure protocol compliance, patient safety, and data integrity
- Manage study supplies, investigational products (IMP), and documentation
- Track site performance, recruitment, and timelines
Quality Oversight
- Apply risk-based monitoring (RBQM) principles
- Ensure compliance with ICH-GCP and regulatory requirements
- Support data cleaning and maintain audit readiness
- Assist during inspections and audits
Stakeholder Collaboration
- Build relationships with investigators, site staff, and stakeholders
- Participate in project meetings and provide operational insights
- Collaborate with cross-functional teams including data management and clinical operations
Documentation & Compliance
- Maintain Trial Master File (TMF) and study records
- Handle adverse event reporting and query resolution
- Ensure accurate and timely documentation of trial activities
Eligibility Criteria
Education
- Graduate degree in Medicine, Pharmacy, Life Sciences, or related field
Experience
- 2 to 4 years of experience as a Clinical Research Associate
- Experience in Phase II–III multinational clinical trials preferred
Skills Required
- Strong knowledge of ICH-GCP guidelines and clinical trial processes
- Experience with EDC, CTMS, and eTMF systems
- Excellent communication and stakeholder management skills
- Strong organizational and time management abilities
- Problem-solving and risk management skills
- Ability to work independently and collaboratively
- Willingness to travel
Salary & Benefits
- Salary: As per company standards
- Opportunity to work on global clinical trials
- Career growth in clinical operations and research
- Exposure to innovative therapies and technologies
- Professional development and training programs
- Inclusive and collaborative work culture
Selection Process
The recruitment process generally includes:
- Online application submission
- Resume shortlisting
- Technical interview
- HR interview
- Final selection
How to Apply
Interested candidates can apply for the Clinical Research Associate at Novo Nordisk role through the official Novo Nordisk careers portal. Upload your updated CV and follow the application instructions.
Important Dates
- Last Date to Apply: April 27, 2026
Why Apply for This Job?
- Work with a globally recognized pharmaceutical company
- Gain experience in multinational clinical trials
- Enhance expertise in site monitoring and regulatory compliance
- Build strong industry connections with investigators and stakeholders
- Opportunity for long-term career growth in clinical research
- Contribute to innovative treatments for chronic diseases
FAQs
1. Who can apply for this job?
Candidates with a degree in Medicine, Pharmacy, or Life Sciences and 2–4 years of CRA experience can apply.
2. Is travel required for this role?
Yes, flexible travel is required for site monitoring activities.
3. What is the salary for this position?
Salary is not disclosed and will be as per company standards.
4. What systems should candidates be familiar with?
EDC, CTMS, and eTMF systems are commonly used and preferred.
5. How can I apply for this job?
You can apply online through the official Novo Nordisk careers website.
Conclusion
The Clinical Research Associate at Novo Nordisk role is a valuable opportunity for experienced CRAs to work on global clinical trials and contribute to impactful healthcare innovations. With strong career growth, international exposure, and a collaborative work environment, this position is ideal for advancing your clinical research career. Apply before the deadline to secure your chance.
Disclaimer
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