Senior Clinical Data Programmer Onconova Therapeutics
Reports to: Senior Director, Data Management
Direct Reports: None
? Provide clinical programming expertise and hands on support to clinical projects.
? Provide strong technical programming support to data management.
? Contribute to activities in validation and implementation including standard reporting systems,
SAS macro utility programs and associated tools.
? Contribute in development and implementation of programming standards and conventions.
? Develop and maintain clinical databases for new and ongoing studies in Medidata Rave and
other systems as needed.
Education, Experience and Skills required for this position:
? A minimum of 12 years hands on relevant work experience in the pharmaceutical or
? Rave Architect certification required. SAS certification preferred.
? Must have a Bachelor?s degree in Computer Science, Mathematics, Statistics, Life Sciences or
? Must have demonstrated experience processing clinical data required for analysis of clinical
? Must have created or acquired tools to improve programming efficiency and quality.
? Must have created and reviewed programming plan and specifications for datasets.
? Needs to be familiar with CDASH and CDISC conventions.
? Able to show that they have established monitoring of data transfers for ongoing trials to
identify study conduct or data quality issues.
? Must have good knowledge of SAS programming.
? Must have strong understanding of clinical trial data and hands on experience in data
? Needs to have a thorough understanding of relational database components and theory.
? Must have excellent oral and written communication skills.
||Pennington, NJ |