Job Description

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Lead Database Facilitation Programmer

Category: Data & AI

Location:

Bangalore, Karnataka, IN

Job Title: Lead Data Facilitation Programmer

Department - CDS GBS

Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment and support your colleagues and stakeholders by challenging the status-quo in a friendly and open-minded way? If so, there is a job opportunity waiting for you as our new Lead Data Facilitation Programmer. At Novo Nordisk, we will challenge you to do the best work of your life. Apply Now.

The Position

As the Lead Data Facilitation Programmer of Data Management and Centralized Data Review at Novo Nordisk, you will be responsible for driving and execution of Health Tracker, EDC and Audit Trail Reports and also any future reports requested by the team at required frequencies. Ensure Data Visualization facilitate visualizations to stakeholders for data review. Perform mapping, testing, creating conversions and supporting the DBL activities across interfaces. In addition setting high goals for personal and group accomplishment, tenaciously working to meet or exceed goals .Programming on Python, R and Power BI with exposure to Clinical Data Management would be added advantage.

The Lead Data Facilitation Programmer key responsibilities :

• Ensure Reports execution of Health Tracker, EDC and Audit Trail Reports at required frequencies. Perform programming, review and update of relevant documents pertaining to reports creation. Facilitate Audit Trail Report in accordance with Risk Based Data Management Guidelines.
• Data Visualisation: Facilitate visualisations to stakeholders for data review. Cater to the trial specific requirements on visualization to stakeholders. Design, develop and maintain data visualization dashboards to help users understand and analyse data.
• Ensure to target opportunities by systematically evaluating project needs, targeting those with the greatest potential for producing positive project results.
• Ensure to works tenaciously to overcome obstacles and to meet or exceed goals; to derives satisfaction from achieving \xe2\x80\x9cstretch\xe2\x80\x9d goals.
• The Lead Data Facilitation Programmer should actively contribute to adequate and timely information of all concerned within and outside of the department.

Qualifications:

• Masters / Bachelor\'s degree in Life Science or comparable degree in computer science, Information Technology clinical information management or equivalent qualifications.
• Minimum 5-8 years of experience in pharmaceutical industry with programming background and preferably 2 years within clinical data management systems
• Understanding of protocol, CRF standards, Inform Terminologies and EDC data structure
• Knowledge and experience in Programming languages such as Python, R & Rshiny
• Knowledge and experience in data visualization tools like Tableau or Power BI
• Knowledge of computer systems, IT and clinical data process flow
• Knowledge of clinical development and basic medical terminology
• Experience in project management, collaboration, communication and presentations skills.
• Profound Knowledge of GxP and guidelines within drug development.

About the Department:

Our Data Management group is 350+ professionals spanning across India, Denmark and North America. Data Management sits in Development where we manage clinical drug development worldwide, ensuring that the process lives up to uniform global standards, regulations and business ethics while delivering viable products that make a difference to patients and ultimately benefit society. Our newly formed Data Review and Cleaning group sits within the Data Management & Centralised Data Review Department led from our Bengaluru site. The Data Review and Cleaning group has been set up to centralise and modernize the data review and cleaning processes, implement new methodologies and to develop innovative toolkits supporting the transformation.

Working at Novo Nordisk

At Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world. Since the company was founded in Denmark more than 100 years ago, we have been translating the unmet medical needs of people living with serious chronic diseases into innovative medicines and delivery. Our focus is on these diseases, which affect hundreds of millions of people and are among the most urgent global health challenges. By combining our innovation and commercial excellence, we draw upon insights from patients and partners to transform bold ideas into life-saving and preventive medicines. Our ambition is to take the lead in each of these areas, driving change with an unfailing belief that it can be done.

Contact

To submit your application, please upload your CV online (click on Apply and follow the instructions)

Deadline

Apply before 20 th Dec, 2023.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we\'re life changing.

Novo Nordisk