.At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.Clinical Data Engineer Purpose:Provide study/standard level technical programming support in collaboration with key stakeholders during setup, conduct and closeout activities.Provide study level support for data structures definitions, monitor quality and standards adherence.Provide study data transformation programming, data loading, data quality checks, data provisioning, and data information flow in the Clinical data environments within a Therapeutic Area or Global Standards Implementation.Scope (global, regional or local):GlobalKey Tasks:- Interpret protocol requirements to translate and document them into study level technical specifications- Develop study level programs for setup, conduct and closeout activities in the clinical data environments- Provision clinical study data to business consumers- Perform data loading / exchange activities (including data exchange with CROs and vendors) and ensure compliance against agreed data transfer specifications- Develop solutions based on gathered requirements from consumers to meet immediate and long-term needs of business customers- Monitor and maintain ongoing study level operations of clinical data environments, respond to study issues- Collaborate with study team functional representatives to ensure a sound understanding of the technical platforms for standardized solutions to study related requests or issues- Ensure adherence to program development, validation and maintenance principals to produce high quality data in line with SOPs, OIs and Best Practice Documents for all data models/environments inclusive of supporting ways to define/enable automation and efficient re-usability- Ensure end-to-end data flow process where traceability requirements are met following Bayer Standards- Complete all documentation associated with programming tasks (e.G. validation, report specifications etc.) in compliance with applicable SOPs and IOs- Estimate the time and resources needed to complete assignments.Track work progress and provide status reports to line manager and studyKey Tasks: team representatives Clinical trials data is a highly regulated and compliance driven environment
