Novo Nordisk is hiring B. Pharma/ M. Pharma/ Pharma D as a Clinical Research Associate – Apply Now

Novo Nordisk is seeking talented professionals with qualifications in B. Pharma, M. Pharma, Pharma D, MBBS, BDS, BAMS, BHMS, B. Sc, or M. Sc for the role of Clinical Research Associate in the dynamic Ahmedabad region. This exciting opportunity allows you to join a global leader in healthcare and contribute to groundbreaking clinical research. If you have a passion for medical science and a commitment to advancing patient care, Novo Nordisk invites you to apply and be a part of their innovative team. Elevate your career with Novo Nordisk and make a meaningful impact in the world of clinical research.

The Clinical Research department at Novo Nordisk India is based in Ahmedabad. We have a team of dedicated professionals working on cutting-edge clinical trials in the field of diabetes and other serious chronic diseases. Our department is fast-paced and dynamic, with a focus on delivering high-quality clinical research projects. Join us and be part of a team that is making a difference in the lives of patients around the world.

Responsibilities

The Clinical Research Associate (CRA) is the primary point of contact between site staff and Novo Nordisk. In this role the CRA acts as ambassador for the company. As a CRA you will be responsible for:

• Taking leadership of site management for the selection (if applicable) and initiation of sites as well as conduction and closing activities of the appointed studies in compliance with local regulations, ICH- GCP, NN procedures and protocol requirements to ensure data quality and study subject protection.
• The CRA is as such responsible for recruitment at site level. The CRA thereby delivers results that have a direct impact on the successful completion of the clinical programme.
  Coordinating with CRM and RTM and communicates to them progress and critical issues that may impair trial progress. In some cases, the CRA may have direct contact with the ITM.
• Efficient and accurate site selection visits (as appropriate including analysis of site logistics, site performance/quality indicators).
• Accountability for patient recruitment strategies, including implementation of mitigation actions.
• Visit trial sites regularly in accordance with the protocol to perform monitoring activities required.
• Proactive use of IT Systems (e.g., IMPACT, EDC) for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team.

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