Under general supervision, performs data management tasks for studies using multiple data sources as well as traditional form-based data capture. Manages timeline; identifies and escalates risk. Designs, documents, and operationalizes data-related work and data flow for these studies; Manages scope and budget.
This is a hybrid position located in San Antonio, TX - we will only consider candidates located in or around the Bexar County area. Responsibilities Perform Data Management tasks at the Associate CRIS level for large, high risk, or complex projects Provide consultative services to clinical investigators regarding methods, minimum standards, and best practices in research informatics. Evaluate, select, and implement data standards for clinical studies.
Relevant standards may include, standard data elements, standard data collection forms, controlled terminologies, common data models, and data exchange standards used in healthcare or research. Maintain Standard Operating Procedures (SOPs) Draft and execute clinical study monitoring plans including site initiation, monitoring and closeout. Serve as the primary point of contact for the study Sponsor and the Principal Investigator for Informatics aspects of clinical studies Assist in developing cost estimates, budget justifications and research plans for data management components of proposals and research grant submissions Collaborate with high level computing and networking staff to design new computer applications for data management processes and solve technical problems that arise Monitor and evaluate existing database management system applications to identify areas for enhancements to improve data quality and the efficiency of data processing Define and maintain detailed functional specifications for new computer applications including user interfaces, data structures, data discrepancy identification and resolution, system interfaces, data processing algorithms, and workflow constraints.
Complete job training requirements for the Intermediate CRIS level. Deliver standard training to new CRISs, review work for activities new to junior CRISs and provide feedback. Other duties as required Qualifications Ability to work in a diverse team environment Strong verbal and written communication skills. and public speaking ability.
Possess strong attention to detail and a penchant for quality workmanship. Strong personal computer skills with working knowledge of Microsoft Office products Ability to work in a multi-tasked matrixed environment Sound knowledge, skills and abilities with data management tools and methodologies. Self-motivated and result oriented; takes ownership for deliverables and deadlines.
Bachelor’s degree in a health profession is required. LICENSES &
Clinical Data Manager (CCDMTM) is preferred. The Association for Clinical Research Professionals (ACRP) Certified Professional (ACRP-CP®) is preferred. Project management certification is preferred.
Full time · 8am-5pm Mon-Fri