Senior Associate - Clinical Study Build Programmer
US: USA Remote
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Overview:
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Position Summary:
The Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data and Analytics colleagues such as the CRF Standards Lead, Clinical Data Manager and other key stakeholders to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.
The ideal candidate will have varied experience in electronic data collection technologies, such as Veeva EDC, Medidata Rave, and Oracle InForm, etc., as well as a sufficient knowledge of industry clinical data standards, the management of CRF library collections, developing CRFs, dynamics and rules, and the integration of third-party data. project management of study deliverables and milestones. The individual will be a self-starter with excellent leadership skills, strong focus on innovation, collaboration, and most importantly, application programming and tools as a representative of data and analytics processes across functional initiatives.
Responsibilities:
- Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components
- Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives
- Provide insights into study level deliverables (i.e. Data Management Plan, Project Plan, database, and observed datasets)
- Contribute to the quality of the data management clinical database programming deliverables including …
This job isn't fresh anymore!
Search Fresh JobsJob Profile
Flexible benefits Vacation benefits
Tasks- Serve as subject matter expert
Application programming CDISC Clinical Data Management Clinical Studies Clinical trials Collaboration Database Programming Data Collection Data Management Data Normalization Data Standards Data Technology Healthcare Innovation Leadership Medidata Rave Metrics Reporting Oncology Organization Programming Project Management Regulatory Guidelines Vendor Management
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9