Vacancy for Clinical Research Associate at Novo Nordisk 2023

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Job Description

Vacancy for Clinical Research Associate at Novo Nordisk 2023. 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.

The CRA is 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.

Organization Novo Nordisk
Post Name Clinical Research Associate
Job Location Mumbai
Official Website https://novonordisk.com/

Job Title/Position:

Clinical Research Associate

Job Overview:

Job vacancy for Science, Pharmacy

Job Location:

Mumbai, Maharashtra

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What are the Key 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.
  • The CRA is 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,
  • The CRA coordinates 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
  • Has good knowledge of trial product and trial protocol and train site staff in trial procedures, handling of trial product and documents
  • Visit trial sites regularly in accordance with the protocol to perform monitoring activities required
  • Proactive use of IT Systems for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team\
  • Guide site staff in preventing deviations that will compromise integrity and quality of trial-conduct

What are the Educational Qualification(s) for Clinical Research Associate?

  • Graduate in Medicine, Science, Pharmacy or other relevant
  • ICH GCP trained and if applicable certified
  • Additional qualification on clinical research would be preferred.

What is the Experience Required for this Job?

  • 2 – 4 years of experience as a CRA
  • Experience in 1-2 multinational clinical trials phase 2-3 from site initiation till site closure.

Related:

Detailed notice

https://careers.novonordisk.com/job/Mumbai-Clinical-Research-Associate-Maha/973196701/

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