Work as Trial Data Programmer in Global Development at Novo Nordisk

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

Post : Trial Data Programmer in Global Development

Job Description
About the department
The data management department was established in Bangalore, India in the month of September 2007 and has significantly grown from 10 members to a strong team of over 119 Clinical Data Management professionals. It is a young, enthusiastic and dynamic team with varied skillsets and professionals from diverse backgrounds such as pharmacy, life-sciences, physiotherapy, computer/information sciences and business administration. The key objective of the department is to ensure high quality data delivery to the stakeholders. The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout.

The position
The position holder will coordinate and ensure timely completion of programming activities with proper documentation and testing for assigned trials/projects following appropriate Standard Operation Procedures (SOPs) and data standards and to the right quality level. The holder will also be responsible for the loading of external data into the clinical database following appropriate SOPs and data standards. Moreover, you will provide business support share better practices and use of standards for procedures and other programming tasks.

The tasks of the Trial Data Programmer will, to a large extent, be performed independently and in accordance with Novo Nordisk SOPs, Novo Nordisk policies and the Novo Nordisk Way. The Trial Data Programmer is recognised as responsible for supporting end users and must act independently, following the strategic objectives of the standards governance bodies and the company in general. The daily work is based in GD-Global Business Services, Bangalore, India. The ability to work in a global context is important, as well as cultural awareness. Some travelling is expected as part of the collaboration as well as for training purposes and international meetings/conferences.

Candidate Profile
• M.Sc/B.Sc in Life Science or comparable degree in Computer Science, Information Technology Clinical Information Management or equivalent qualifications
• Minimum 2-3 years of experience in pharmaceutical industry and preferably 1 year within Clinical Data Management Systems
• Good Programming Skills
• Preferably 1 years of experience in Information Technology
• Knowledge of clinical development and basic medical terminology
• Experience in project management, collaboration, communication and presentations skills
• Experience in supervision and mentoring
• Knowledge of GxP and guidelines within drug development

Additional Information
Qualification : M.Sc/B.Sc
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Global Development
End Date : 25th March, 2020