Job Description

Job description Department- Trial Data Management 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-r

Job description Department- Trial Data Management 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 Associate Lead Data Manager. At Novo Nordisk, we will challenge you to do the best work of your life. Apply Now. The Position: The Associate Lead Data Manager is expected to serve as a CTDM point of contact for complex trials (including new data sources) or across multiple trials. Alternatively, being specialised in a business-critical process or system and capable of applying this expertise across multiple trials. Mentor more junior colleagues and contribute with an innovative mindset that challenges the status quo. The Associate lead Data Manager Will be responsible for: Participate in and provide input to protocol outline and protocol development. Define the structure and specifications for data collection in collaboration with internal and external stakeholders (CRF, external data). Supervise the setup of clinical data management systems and interfaces. Create, maintain, and put into action a Data Management Plan that covers all data management activities and oversee the creation of a trial data quality plan (data checks, blinding). Ensure clear and concise communication with operational and functional trial partners (e.g., Data Management Systems and Standards, Biostatistics, Trial Operations, Medical & Science, Clinical Supplies, Global Safety), as well as timely follow-up. To review / understand data and make operational decisions, use data visualisation methods. The Associate Lead Data Manager will perform post- Database Lock (DBL) activities to ensure submission-ready data and resolve or escalate major issues, with assistance from the Manager of the relevant data management unit. Qualifications: M.Sc. /B.Sc. in Natural/Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical information management or equivalent qualifications. A degree in computer science or equivalent professional experience. 3-10 Years of experience in pharmaceutical or development industry and preferably with an end to end exposure in Clinical Data Management. Excellent knowledge of clinical systems used in drug development, in the field of relational database systems. Experience working under quality requirements such as GCP and ISO, Clinical development, and Project Management. Excellent written and spoken English. Ability to plan well and handle complex tasks simultaneously and independently. Analytical and result oriented. Good team player with communication and stakeholder management skills. Proactive and resilient to changes. Aboutthe Department : The Trial data management department was established in Bangalore, India in the month of September 2007 and has significantly grown. 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. 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). Please take note that this position is only open to external applicants. It is requested that internal candidates not apply. Deadline Apply before 20th September,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.