Senior Clinical Trial Data Manager

2 weeks ago


Bengaluru, Karnataka, India Novo Nordisk Full time

Department: Data Management & Centralised Data Review

Ready to take on a challenging Senior Clinical Trial Data Manager role? Experienced in clinical trial data management and dedicated to ensuring high-quality data delivery? Join our Data Management & Centralised Data Review team in Bangalore, India, and make a valuable impact in the healthcare field. Read on for an opportunity to embark on a rewarding career.

The Position

The Senior Clinical Trial Data Manager has a wide range of responsibilities, managing global data review activities efficiently and proactively addressing new challenges. This role also involves project management for data review and ensuring comprehensive trial data review delivery from data management.

As a Senior Clinical Trial Data Manager at Novo Nordisk, you will:

  • Lead data review project management and oversee clinical trial data review tasks.
  • Ensure end-to-end data review delivery, meeting project goals and plans effectively.
  • Manage the entire data review process, identifying project risks and facilitating decision-making.
  • Ensure clinical data complies with regulatory and quality standards.
  • Implement data review tools and interfaces, and execute a data Monitoring Plan.
  • Conduct database lock activities for submission-ready data and maintain clear communication with trial partners.

Qualifications

To excel in this role, you should have:

  • MSc/BSc in Natural/Life Science or related field.
  • 4 - 6 years of data management experience, preferably in the Pharma Industry.
  • Excellent knowledge of clinical systems and relational database systems.
  • Strong expertise in data systems management, analysis, and quality assurance.
  • Proficiency in data acquisition, transformation, and regulatory submission.
  • Familiarity with data management tools, trial regulations, and data governance.
  • Understanding of data architecture and business communication.
  • Experience with Good Clinical Practices (GCP) and/or Good Laboratory Practices (GLP).
  • Knowledge of drug and disease terminology and reviewing research protocols.

About the Department

Our Clinical Data Operations group comprises 400 professionals globally. Data Management in Development oversees clinical drug development worldwide, maintaining global standards and delivering impactful products. Our Data Review and Cleaning group, part of the Data Management & Centralised Data Review Department, focuses on modernizing data processes and implementing innovative toolkits.

Working At Novo Nordisk

Novo Nordisk, a leading global healthcare company, is renowned for combating chronic diseases. With a commitment to impacting millions of lives daily, we strive for excellence and inclusivity, ranking among the world's top companies. Our success hinges on the collaboration of our diverse 63,000+ workforce. At Novo Nordisk, we foster a culture that values individual perspectives and continuous innovation. Join us as we work together towards meaningful change.



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