Senior Clinical SAS Programmer

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At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better - join our team today! Your Role: Senior Clinical SAS Programmer This position is expected to be highly influential in partnering with product development teams and third parties to develop data management strategies that result in on-target delivery of final databases. This position will closely collaborate with R&D functions including clinical development, internal study sites, biostatistics, regulatory affairs, and quality assurance to ensure data integrity, data quality, validation, and compliance Your Responsibilities: - Proactively search for solutions. Work effectively and flexibly within and across all Elanco R&D teams and external collaborators to achieve overall Elanco R&D deliverables. Create a positive work environment that is aligned with company objectives. Provide and accept challenge to deliver innovative technical solutions and create an innovative culture. Create an engaging culture with a "Play to Win" mentality. Identify and utilize methods to deliver individual objectives in a high quality, timely, cost-effective manner. Demonstrate high levels of adaptability, flexibility, and learning agility Key Technical Responsibilities Use SAS or other software to develop custom programming reports helping in data cleaning activities. Ensure that outputs meet quality standards and project requirements. Perform validation programming and work with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings. Ensure adherence to clinical data collection policies and procedures and is expected to keep Elanco at the forefront of standards for the animal health industry Keep project team members informed of programming progress and issues requiring their attention. Confirm validation and compliance to all regulations (including GxP) and guidelines the global data management systems and process utilized to collect, manage, report, store and archive databases containing clinical data Be part of the regular connects with site lead and study team (Site/Study program leads). Manage scheduling and time constraints across multiple projects at a time, set goals based on priorities from management, and adapt to timeline or priority changes by reorganizing daily workload. Prepare in advance for internal meetings, contribute ideas, and demonstrate respect for opinions of others. Negotiate and establish accurate time estimates for completion of study programming activities with internal team members. Assist in drafting regulatory submissions. Ensure scientific integrity and animal welfare in all activities. Create and maintain standard macros and applications to improve the efficiency of the department. Develop wider knowledge of SAS and other relevant programming languages and processes within the Data Management, Biostatistics and Medical arenas. Contribute to the mentoring of other programmers, developing training courses, presenting training materials, providing feedback, or guiding new associates in process. Participate in internal/external audits and regulatory inspections as required. Engage in knowledge share activities What You Need to Succeed (minimum qualifications): - BSc / MSc in related fields - Minimum 10 years of relevant experience (some vaccine development experience will be a plus) - Expertise in SAS programming with associated basic and advance certifications. - Strong GxP knowledge, in particular GLP, GCP and GMP. - Good written and verbal communication skills What will give you a competitive edge (preferred qualifications): - Clinical trial experience and/or clinical trial data experience - Knowledge of electronic data capture systems - Experience interacting with regulatory authorities and regulatory submissions - Ability to communicate logically and technically. Deliver all communication with clarity, impact and passion tailored to the audience. - Organizational planning skills, ability to manage competing priorities and flexibility to change. - Commitment to quality. - Ability to work independently or as part of a team. High competency in Microsoft Office. Additional Information: Travel: 0% Location: India, Bang