EDC programmer working on initial study build as well as post production changes.

> Develop and maintain trial specific database applications.> eCRF Building in InForm (Phase Forward), Central Designer Software (electronic data capture) tools. Scripting rules for data in eCRFs i.e. Rules (edit check) development in INFORM and Central Designer. Develop electronic clinical data management (eCDM) systems (eCRFs, edit checks, visit structures, system settings, role assignments, etc.). Review specifications to assure the requirements are clear and appropriate. Understand, and apply Client standards library to each study build. Conduct change and proper version control process for requested and approved changes to production studies. Maintain issues logs and seek issue resolutions to assure delivery on time. Attend and participate in eCDM team meetings. Increase depth of knowledge of the clinical trials process and industry and technical eCDM expertise. Maintain appropriate documentation as required by SOPs. Perform all tasks as required by SOPs.> Coordinate with project team to successful completion of a project within given timelines and budget. > Understand and deliver the trials to customer in both the Fast Start and Fast Forward phases of trial.> Setup the Data base, tasks include development of eCRF, Edit Checks, Admin Module, documentation, TDE setup and Cognos Reports (based on Sponsor requirement).> Analysis, Design, Code Development, Code Review and Testing of various modules.> Analyze and implement the desired change as per customer specification by constant interaction with data management department and customer.

InForm\SAS programming

Marketing + Business Development

Marketing