Novo Nordisk is inviting applications for the Clinical Research Associate (CRA) position in Delhi, India. This opportunity is ideal for professionals with 2โ4 years of clinical research monitoring experience who want to contribute to global Phase IIโIII clinical trials and innovative drug development.
The CRA role at Novo Nordisk is part of the Site Monitoring Excellence team, responsible for overseeing clinical trial sites, ensuring ICH-GCP compliance, patient safety, and high-quality clinical data. Candidates will collaborate with investigators, clinical teams, and regulatory stakeholders to ensure successful clinical trial execution.
With Novo Nordiskโs strong focus on diabetes, obesity, and chronic disease research, this role provides a chance to work in a global clinical development environment and gain exposure to advanced risk-based monitoring strategies.
Key Responsibilities โ Clinical Research Associate
Site Management & Monitoring
- Act as the primary liaison between Novo Nordisk and clinical trial sites.
- Conduct on-site and remote monitoring visits according to the Monitoring Plan and ICH-GCP guidelines.
- Monitor patient safety, adverse events, and data integrity.
- Manage clinical queries and resolve discrepancies in trial data.
- Track site performance, recruitment, and retention metrics.
- Ensure proper Investigational Medicinal Product (IMP) accountability.
- Maintain documentation in the Trial Master File (TMF).
Quality Oversight
- Implement Risk-Based Quality Management (RBQM) practices.
- Support data cleaning and clinical data flow plans.
- Maintain inspection readiness for audits and regulatory inspections.
- Ensure compliance with ICH-GCP, regulatory requirements, and internal SOPs.
Stakeholder Collaboration
- Work closely with investigators, clinical coordinators, and key opinion leaders.
- Collaborate with internal teams including Trial Managers, Data Management, and Clinical Operations.
- Participate in investigator meetings and training programs.
Eligibility Criteria
Educational Qualification
Candidates should have a degree in:
- Pharmacy (B.Pharm / M.Pharm)
- Life Sciences
- Medicine or related healthcare discipline
Experience Required
- 2โ4 years of experience as a Clinical Research Associate (CRA)
- Experience in multinational clinical trials (Phase IIโIII)
- Experience covering site initiation to site close-out
Required Skills
Applicants for this CRA job in Delhi should possess:
- Strong knowledge of ICH-GCP guidelines
- Understanding of clinical trial methodology and regulations
- Experience with EDC, CTMS, and eTMF systems
- Excellent communication and stakeholder management skills
- Strong project management and risk mitigation abilities
- Ability to manage multiple clinical trial sites simultaneously
Why Join Novo Nordisk?
Working with Novo Nordisk clinical research teams offers several benefits:
- Opportunity to work on global clinical trials
- Exposure to innovative medicines for diabetes and chronic diseases
- Professional development in clinical research and regulatory compliance
- Collaborative international work environment
- Career growth in clinical development and monitoring excellence
Job Location
Delhi, India
Application Deadline
20 March 2026
How to Apply
