Clinical Programmer

You will be responsible for supporting all statistical programming, data review reporting, and analytics development aspects of assigned studies or project-level activities. Your role will involve producing and tracking reports for various line functions within Global Drug Development to monitor clinical data continuously. You will provide understandable and actionable reports on clinical data to key stakeholders and facilitate interaction with end-users in creating specifications and performing programming activities for successful delivery. In addition, you will provide quantitative analytical support to global program teams, support the planning, execution, and close-out of Clinical Programs/Trials, and collate and deliver analytics reports for critical decision-making. You will also create, file, and maintain appropriate documentation, work with internal subject matter experts and key stakeholders to provide analysis and interpretation of clinical program/trial operational data, and offer necessary training to end-users on the best and consistent use of various data review tools. Your key responsibilities will include programming reports of various complexity from documented requirements within the clinical reporting systems using SQL, PL/SQL, C#, VB script, SAS, Python, and R. It is essential to have a good understanding of Novartis Clinical Data Standards and their implementation for the creation of report specifications or outputs. Your performance will be measured based on the quality and timeliness of deliverables, revisions caused by logic or programming errors, and customer feedback and satisfaction. The minimum requirements for this role include 2-5 years of experience in clinical review and reporting programming, business analytics, and/or clinical trial setup in the pharmaceutical, CRO, or Life Science related industry. You should also have a strong knowledge of programming languages, data review tools, clinical data management systems, attention to detail, time management, customer focus, ability to translate technical concepts for non-technical users, and strong verbal and written communication skills. Moreover, you need to understand Drug Development Process, ICHGCP, CDISC standards, and Health Authority guidelines and regulations. Novartis offers a collaborative and supportive environment where smart and passionate individuals like you can make a difference in patients" lives. If you are ready to contribute to creating a brighter future, consider joining our Novartis Network and explore suitable career opportunities. Additionally, Novartis is committed to providing reasonable accommodation to individuals with disabilities. If you require accommodation during the recruitment process, please contact [email protected] with your request and contact information.,