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Clinical Research Associate Job Vacancies at Novo Nordisk

Explore exciting career opportunities with Novo Nordisk, a global leader in diabetes care, as we strive to defeat diabetes and address serious chronic conditions. Join our high-performing team in Ahmedabad, Gujarat, and play a pivotal role in driving business success. This blog post introduces job vacancies for the position of Clinical Research Associate (CRA) at Novo Nordisk, focusing on the Clinical Medical Regulatory (CMR) department.

Novo Nordisk

Novo Nordisk, a Denmark-based multinational, holds leadership in diabetes care. With a commitment to defeating diabetes and other chronic conditions, Novo Nordisk’s innovative biological medicines benefit millions of people worldwide. The India affiliate office, located in Bangalore, comprises over 1,400 professionals working across various functions. Joining Novo Nordisk means being part of a transformative journey to translate unmet medical needs into life-saving and preventive medicines.

Company Vacancies List

• Position Title: Clinical Research Associate
• Location: Ahmedabad, Gujarat, India
• Department: Clinical Medical Regulatory (CMR)

Job Description

As a Clinical Research Associate (CRA) at Novo Nordisk, you will be the primary point of contact between site staff and the company. Your responsibilities will include:

• Leading site management for study selection, initiation, conduction, and closing activities.
• Ensuring compliance with local regulations, ICH-GCP, NN procedures, and protocol requirements.
• Coordinating with Clinical Research Managers (CRM) and Regional Trial Managers (RTM) and communicating progress and critical issues.
• Conducting efficient and accurate site selection visits, analyzing site logistics, performance, and quality indicators.
• Taking accountability for patient recruitment strategies, implementing mitigation actions, and regularly visiting trial sites as per the protocol for monitoring activities.
• Proactively using IT Systems (e.g., IMPACT, EDC) for site visits and source data verification in collaboration with the data management/logistics team.

Qualifications

• Graduate in Medicine, Science, Pharmacy, or a relevant field.
• ICH-GCP trained and, if applicable, certified.
• Additional qualifications in clinical research are preferred.
• 2-4 years of experience as a CRA.
• Experience in 1-2 multinational clinical trials (phase 2-3) from site initiation to closure.

About the Department

The Clinical Research Associate (CRA) role reports to the Clinical Operations Manager (COM) and is vital in maintaining a strong connection between site staff and Novo Nordisk. The CRA is accountable for patient recruitment strategies, implementing mitigation actions, and regularly visiting trial sites to perform required monitoring activities.

Working at Novo Nordisk

At Novo Nordisk, we are committed to driving change and transforming bold ideas into life-saving and preventive medicines. Our focus on diabetes, obesity, and rare blood and endocrine diseases aligns with some of the most urgent global health challenges. Join us as we combine innovation and commercial excellence, working collaboratively with patients and partners to make a significant impact.

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