Associate Lead Data Facilitation Programmer

1 week ago

Bengaluru, Karnataka, India Novo Nordisk Full time

Department: Clinical Drug Development - Global Business Solutions

Are you passionate about ensuring quality and simplifying processes? Do you have the innovative mindset to drive change in a forward-thinking environment and support your team by challenging the status quo in a collaborative way? If so, we have an exciting job opportunity for you as our new Associate Lead Data Facilitation Programmer at Novo Nordisk where we will push you to excel. Be part of a team that values your input and encourages growth.

The Role

As the Associate Lead Data Facilitation Programmer in Data Management at Novo Nordisk, you will be in charge of executing Health Tracker, EDC, and Audit Trail Reports as well as any future reports as needed. You will ensure that Data Visualization aids stakeholders in data review. Additionally, you will be involved in mapping, testing, conversions, and supporting DBL activities across interfaces. Knowledge of programming languages like Python, R, and Power BI, along with exposure to Clinical Data Management, will be beneficial for this role.

The key responsibilities of the Associate Lead Data Facilitation Programmer include:

  • Execute Health Tracker, EDC, and Audit Trail Reports as required. Review and update relevant documents related to report creation. Facilitate Audit Trail Report based on Risk-Based Data Management Guidelines.
  • Create interactive dashboards using Python or R for real-time clinical data monitoring. Customize visualization as per trial requirements. Develop and maintain data visualization dashboards for data analysis.
  • Manage data systems to consolidate information from various sources. Implement data pipelines for efficient processing while ensuring data integrity and timeliness.
  • Collaborate with various teams to define requirements and deliver data solutions. Effectively communicate data insights to non-technical team members. Maintain well-documented codebases and follow secure coding practices.

Qualifications:

  • Master's / Bachelor's degree in Life Science or related field
  • 5-8 years of experience in pharmaceutical industry with a programming background
  • Understanding of protocol, CRF standards, EDC data structure
  • Proficiency in Python, R & Rshiny
  • Experience with data visualization tools like Tableau or Power BI
  • Knowledge of IT systems and clinical data flow
  • Experience in project management and communication skills
  • Understanding of GxP principles within drug development

About the Department:

Join our Data Management team of over 350 professionals globally, where we oversee clinical drug development to ensure adherence to global standards and ethics. Our emphasis is on delivering impactful products while upholding regulations. Be part of the Data Management & Centralised Data Review Department at Novo Nordisk's Bengaluru site, focusing on centralizing and enhancing data review processes to drive innovation.

Working at Novo Nordisk

Novo Nordisk, a prominent healthcare company, is committed to making a difference in patients' lives worldwide. Our growth and dedication have earned us a place among the top global companies. With over 63,000 employees, we value diversity and continuously strive to harness our employees' unique strengths. Join us in our mission to create a positive impact together. Let's go further, together.

Contact:

To apply, upload your CV on the provided platform. Application deadline: 30th May, 2024.

We believe in fair recruitment practices and equal opportunities for all applicants. At Novo Nordisk, we aim not just to be the best company in the world, but the best for the world. Join us in fostering an inclusive culture that celebrates diversity and promotes positive change.

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