Veeva Configuration

2 weeks ago

India Predactica™ Full time

Predactica, an AI/ML product based startup company is looking for a Viva certified developer in India for one of its clients.


As a DevOps Engineer, you will be accountable for developing, optimizing, and managing IT services/applications in Veeva with focus on Clinical trial management. You will also focus on ensuring cost-effectiveness, scalability, and security in all aspects of the digital product lifecycle, including maintenance activities. As part of enterprise engineering, you will be involved in understanding the business application processes and functions.


Key Responsibilities

__________________

  • Lead, collaborate, and facilitate cross-functional experts to deliver a particular solution with a good understanding of the business requirements.
  • Responsible for the quality of the technical deliverables which also includes peer reviews.
  • Develop and publish the application/prototype with the knowledge of DevOps according to the underlying infrastructure.
  • Lead the implementation and maintenance of efficient Continuous Integration / Continuous Delivery pipelines to automate the delivery process.
  • Act as a subject matter expert for Veeva to support the design, implementation and maintenance of reliable and performant integrations.



Qualifications and experience

_________________________


  • Understanding of Veeva's architecture, data models and integration methods.
  • Proficiency in configuration tools and methodologies specific to Veeva.
  • Knowledge of integration mechanisms, data flow and efficient communication between applications.
  • Approaching challenges with a consulting mindset being flexible to adapt to changes and uncertainty.
  • Certification of the Veeva platform will be value-added.
  • Clinical Domain Knowledge: Understanding of clinical trial processes, regulatory requirements, and standards like Good Clinical Practice.
  • Essential effective oral and written communication skills in English.
  • Working knowledge of Computer Systems Validation (CSV) and GxP.
  • Working knowledge of regulations like HIPAA and GDPR in the healthcare industry.
  • Moderate travel is required and the ability to work across multiple time zones.
  • 3-5 Years of relevant work experience with Bachelor’s degree in Computer Science/IT/Engineering or 5 – 7 Years of relevant work experience
  • At least 3+ years experience of working in one or more multinational work environments (e.g. life science industry experience is a plus).

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