Clinical ProgrammerCatalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com.    As a Clinical Programmer you will be a key member of the Development Operations, Data Management Team. You will be responsible for program standard and study specific electronic Case Report Forms (eCRFs), edit checks and reports in accordance with approved Database Specifications, Data Management Plans (DMP), Data Transfer Specifications (DTS) and Data Review Specifications (DRS). Set-up study specific mapping for WHO-Drug and MedDRA dictionaries. Provide clinical programming support for data cleaning in clinical trials based on Standard Operating Procedures (SOPs) or study specific guidelines.