A company is looking for a Database Designer (Clinical Trials).
Key Responsibilities
Designing CRFs for regulatory submission and conducting CRF annotation activities
Developing and validating databases in CDMS, including preparation and review of relevant documentation
Extracting data from clinical data management systems and supporting data management tasks
Required Qualifications
Post-Graduate degree in Pharmacy, Science, or Computer Science is preferable
Minimum of 5 years of experience in clinical data management within the Pharma / CRO industry
Experience in database development and clinical programming
Proficiency in EDC tools such as Octalsoft, CRONOS, Medidata Rave, Inform, or Oracle
Clinical Trial • Houston, Texas, United States