Job Description

Job description Department: Centralised Monitoring Unit, CDS GBS - Bangalore Are you passionate about what you are doing Do you want to build excellence within processes in the most efficient way Do you have an innovative mindset to drive change in a future-ready environment Are you best at what you do If so, raise your hand as there is an exciting opportunity waiting for you as \'Clinical Data Programmer\' with us. \'Apply Now\'At Novo Nordisk, we assure you will experience the best. About the department Bangalore Global Development since its inception, has transitioned from a small start-up to one of the largest units in Global Business Services, Bangalore (GBS) and a key contributor to Novo Nordisk clinical development portfolio. The Centralised Monitoring Unit (CMU) was established in GBS in 2016 to support the Risk Based Monitoring of clinical trials conducted by Novo Nordisk in line with health authority requirements. The unit is the single and only entity across the globe responsible for performance of centralised medical monitoring for all clinical trials involving medical review of patient data that includes medical monitoring and lab surveillance and generation of visualisations and reports identifying outliers and trends from various data sources. The Position An Associate Functional Programmer will be responsible to Generate Standard and custom Trial Monitoring reports to support Risk Based Monitoring (RBM) across the trial portfolio and Prepare and Maintain report-related documentation with engagement in Trial Monitoring report meetings. Understand stakeholder needs on Trial/Medical Monitoring and Risk Indicator reports and pre-pare specifications. Program new and / or customize existing programs as per specifications using programming language e.g.: SQL / PLSQL / SAS / JMP etc., that utilize data from multiple source such as IMPACT, OC, CDW, IWRS, ePRO etc. Generate standard/or customize existing reports as relevant for e.g., Projects, Study Groups, Management, Titration group, Data Review group etc. Generate ad-hoc reports e.g.: AESI, Data Cleaning cycles, Protocol deviations, Site Data Entry status, Subject lists etc., for stakeholders. Familiar with reporting platforms such as Qlik Sense, SAS Visible Analytics, Business Objects (SAP) etc. Experience M.Sc./B.Sc. in Life Science or comparable degree in computer science, Information Minimum 1- 3 years of experience in pharmaceutical industry and preferably 1 year within Clinical Data Management systems, Bioinformatics or Clinical Research Associate. Knowledge of validation of computer systems. Knowledge of drug development and basic medical terminology. Profound knowledge of GxP and guidelines within drug development Technical skills: ability to see technical solutions matching specific data or data base challenges. Basic knowledge in one programming language such as VBScript / SAS / SQL/PLSQL. Familiar with one or more of the following reporting platforms such as Business Objects (SAP), SAS Visible Analytics, Qlik Sense, SAS JMP clinical. Excellent communication and collaboration skills (written/verbal). Working At Novo Nordisk At Novo Nordisk, we don\'t wait for change. We drive it. We\'re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales- we\'re all working to move the needle on patient care. Contact To submit your application, please upload your CV online (click on Apply and follow the instructions). Internal candidates are kindly requested to inform their line Manager before applying. Deadline 05th June 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.

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