CDM Programmer II

Work Schedule

Environmental Conditions

Job Description

Company Name:                                              PPD Development, L.P.

Position Title:                                                   CDM Programmer II

Salary:                                                               $75,900.00 - $126,500.00 per year

Location:                                                           929 North Front Street, Wilmington, NC 28401

Summary of Duties: Perform tasks following within the timelines established by the team, in accordance with the process outlined in the departmental procedures and indicated by the project contract. Design, build and test project databases and edit checks. Define and import data into the system. Define, create and test listings for data review and perform programming activities in line with project requirements. Act as the lead on studies of simple to moderate complexity with close supervision. Research and leverage resources to resolve issues and manage moderately complex tasks through the development and application of new knowledge and professional skills in areas including programming and technology. Participate in process improvement initiatives to increase efficiencies. Increase knowledge and skills to gain good understanding of the lead programmer roles and overall department processes. Ensure adherence to departmental working practice documents and SOPs, and contribute to the development of informal training materials. Duties may be performed remotely.

Qualifications: Bachelor’s degree in Health Informatics, Bioinformatics, Data Science, Information Systems, or related field and two (2) years of experience as a CDM Programmer II, Clinical Data Programmer, involving clinical trial data programming, or related role involving clinical trial data programming. Must have two (2) years of experience with: Programming languages: SAS, SQL, C#; Relational database systems (RDBMS) and structure: Oracle, MySQL; SAS software modules: Base SAS, SAS/STAT, SAS/GRAPH, SAS macro, SAS ODS, SAS SQL; SQL, Crystal Reports, and JReview; Microsoft Word to produce relevant study documentation; Microsoft Excel to manage and exchange study data; and Microsoft Project to manage timelines and resourcing of projects. Must have one (1) year of experience with: CDMS Clinical Data Management Systems: Medidata Rave, Veeva CDMS, Oracle Inform.