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Venesco LLC is seeking a Clinical Database Developer to lead design, development, testing, validation, and maintenance of clinical trial databases for FDA-regulated programs. You will ensure compliance with FDA regulations, ICH guidelines, GCDMP and CDISC standards, while supporting data collection, quality control, and regulatory submissions.
The role focuses on EDC database work, CRF development, UAT, and collaboration with Trial Managers, Data Managers, SAS Programmers, and Biostatisticians
Description
Venesco LLC is seeking a Clinical Database Developer to serve as the technical lead for the design, development, testing, validation, implementation, and maintenance of clinical trial databases supporting FDA-regulated medical product development programs. The individual ensures clinical databases meet FDA regulatory requirements, ICH guidelines, Good Clinical Data Management Practices (GCDMP), and CDISC standards, while supporting data collection, quality control, and regulatory submissions.
Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.
For more information on Venesco, LLC., visit https://venesco.com.