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Require Clinical Research Associate at Novo Nordisk

 

 

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Require Clinical Research Associate at Novo Nordisk

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.  

Post : Clinical Research Associate - Pipeline

Job Description
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.

Candidate Profile
• You should be graduate in Medicine, Science, Pharmacy or another relevant field preferred.
• Certified in ICH GCP trained is preferred.
• Additional qualification on clinical research would be preferred.
• 2 - 4 years of experience as a Clinical Research Associate.
• Experience in 1-2 multinational clinical trials phase 2-3 from site initiation till site closure preferred.


Additional Information
Experience : 2 - 4
Qualification : Graduate in Medicine, Science, Pharmacy
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Development
End Date : 30th August 2024

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