Assist with the development, testing and implementation of clinical research databases. Organize data to analyze, identify and report trends. Review Case Report Forms (CRFs) for accuracy and completeness.
Process laboratory and other external data. Review reports, tables, and listings.
Prepare reports of clinical research data for internal validation and cross validation for data quality efforts. Evaluate and resolve issues regarding contents of reports.
Support the data management process for clinical research projects by assisting in the development of data management documentation and guidelines
Perform quality checks to ensure accuracy of data manually entered by others. Maintain and audit data, providing status and activity reports as required. Consult with senior peers on non-complex projects to learn through experience.
May perform clinical data entry and validation to ensure accuracy, completeness and legibility of data. Assists with the development and evaluation of clinical record forms. Maintains internal record keeping system(s) in conjunction with clinical research associates and biostatistics internal staff. Maintains master files for clinical protocol.
Effective verbal, written, interpersonal and telephone communication skills. Very strong written and oral communication required.
Ability to relate to diverse age and demographic backgrounds.
·Attention to Detail
Strong attention to detail and problem solving.
Computer literate and working knowledge of software applications (word processing, spreadsheet and database). Demonstrate diplomacy, tact and a professional demeanor.
Knowledge of medical terminology.