Job title: Senior Clinical Data Programmer

Company: Novo Nordisk

Job description: Job description “Starting a career at Novo Nordisk is more than getting a job. It is an opportunity to improve the lives of millions of people living with a serious chronic disease. We are a proud life-science company on a mission to ensure that pe

Job description ‘Starting a career at Novo Nordisk is more than getting a job. It is an opportunity to improve the lives of millions of people living with a serious chronic disease. We are a proud life-science company on a mission to ensure that people living with a chronic disease can live a full life. Millions rely on us. It is very important to us that anyone working with us feels empowered as an employee and as a person. We all should have the opportunity to act fast, make decisions and be agile. We are looking for a potential candidate in our Data Systems & Automation, Clinical & Data Science GBS (DSA, CDS GBS) unit who will be responsible Design and set-up of study database for data collection in clinical trials based on protocol needs and Process. The position is based in Bangalore. The position A Senior Clinical Data Programmer – DMW, you will be responsible for end-to-end clinical data management activities focus areas to internal and external stakeholders… Design and set up of study database for data collection in clinical trials based on protocols needs Set up of models and performing transformation updates in DMW Mapping of metadata and clinical data from source system(s) to DMW (Data Management Workbench) / CDW (Clinical Data Warehouse) and generate SDTM (Study Data Tabulation Model deliverables. Active participation in sharing better practices on use of standards in alignment with Lead Clinical Data Programmer and Process & Automation Specialist. Maintain system related documentation. Facilitate implementation of business processes introduced by the systems supported by DaMaSys (Data Management Systems & Standards). Ensure testing is performed and database meets specification requirements before deployed into production and document pass and fail scenarios in a timely manner. Design, Programming and validate programs to check data accuracy and aid report generation This position requires you to be highly self-motivated, proactive, organised and have excellent stakeholder management, communication skills. Ensure quality of submissions by complying to procedures and systems. Qualifications Below are the required skills. Ph.D. with substantial clinical and/or research expertise relevant area preferred PharmD and MPharm with relevant experience could be considered 5-7 years of relevant work experience Understanding of the pharmaceutical industry Fluency in both spoken and written English Demonstrated research experience (e.g. publications) Additional education and experience in medical communication Study or work in a country other than the native country Working at Novo Nordisk At Novo Nordisk, we strive for excellence. You share the same passion and commitment as our employees in our journey to make a difference to patients’ lives. In exchange, we offer you the chance of a lifetime to work with extraordinary talent and benefit from unmatched opportunities for professional and personal development. Contact To submit your application, please upload your CV online (click on Apply and follow the instructions). Deadline 15 June 2022 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.

Expected salary:

Location: Bangalore, Karnataka

Job date: Thu, 02 Jun 2022 22:11:51 GMT

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