Clinical Research Associate Job at Novo Nordisk | Apply Now
A Clinical Research Associate job is an excellent opportunity for professionals interested in clinical trials and innovative healthcare research. Novo Nordisk, a global healthcare company known for its strong commitment to improving patient lives, is offering a promising career opportunity in Delhi. This role allows experienced clinical research professionals to contribute to high-quality clinical trials, ensuring patient safety, data integrity, and compliance with global research standards. If you are looking for Novo Nordisk careers or a rewarding medicine job in clinical development, this position could be the perfect next step in your career.
Job Details:
- Job Position: Clinical Research Associate (CRA)
- Location: Delhi, India
- Department: CDC India – Clinical Development
About the Company:
Novo Nordisk is a global healthcare company with a strong heritage in research and development and a clear commitment to improving patients’ lives. The company focuses on developing innovative medicines for chronic diseases such as diabetes, obesity, and other serious conditions.
Working at Novo Nordisk means being part of a truly global workplace where dedication, innovation, and patient-centric research drive progress. Professionals seeking Novo Nordisk careers gain access to an environment that promotes learning, collaboration, and professional growth.
Job Description:
The Clinical Research Associate job involves providing strategic oversight and management of clinical trial sites to ensure protocol compliance, data integrity, and protection of patient safety and rights. The CRA plays a critical role in executing high-quality clinical trials by implementing risk-based monitoring and proactive risk management strategies.
This medicine job requires working closely with site staff and cross-functional teams to ensure successful study execution, maintain regulatory compliance, and support the development of innovative medicines.
Qualifications:
- Graduate in Medicine or other relevant discipline.
- Minimum 2–4 years of experience working as a Clinical Research Associate.
- Experience in 1–2 multinational clinical trials (Phase II–III) from site initiation to site closure.
Skills and Competencies
- Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial methodology.
- Proven track record of delivering high-quality clinical trial execution.
- Excellent stakeholder management and communication skills.
- Ability to work independently and collaboratively in dynamic environments.
- Strong organizational and time management skills to manage multiple sites or studies.
- Project management skills with attention to detail and commitment to patient safety.
- Proficiency with EDC, CTMS, eTMF, and other clinical systems.
- Strong problem-solving and proactive risk-management abilities.
- Willingness to adopt new digital tools and continuous improvement practices.
- Flexibility to travel when required.
Key Responsibilities:
- Manage assigned clinical trial sites and act as the primary liaison with site staff and study teams.
- Conduct on-site and remote monitoring visits in compliance with protocol, ICH-GCP, SOPs, and regulatory guidelines.
- Ensure patient safety, data integrity, and timely reporting of queries and adverse events.
- Track site performance, recruitment, retention, and data delivery to meet study timelines and quality standards.
- Oversee investigational product (IMP), study supplies, essential documents, and site equipment accountability.
- Provide site training and operational support on protocols, systems, and compliance requirements.
- Maintain accurate trial documentation and ensure Trial Master File (TMF) compliance.
- Apply Risk-Based Quality Management (RBQM) to identify and mitigate study risks.
- Support data cleaning, audit readiness, and regulatory inspections.
- Collaborate with investigators, site teams, and cross-functional stakeholders to improve study performance.
Application Deadline: March 20, 2026
