Location : Wilmington, DE [On-Site] Employment Type : Direct Hire Job ID : 7247 Date Added : 02 / 20 / 2020 Thank you for applying. Someone will be contacting you shortly. Uploading Data... Creating Application... Finishing up... A new application was submitted.
The Lead Biostatistical Programmer I is responsible for processing clinical data required for statistical analysis of Phase I — III clinical trials, and leading project teams.
Qualifications
Bachelor’s degree in Statistics, Mathematics, Computer Science or health related field. Masters is preferred.Minimum 5 years of programming experience using SAS Base / Stat / Macro / GRAPH in the biopharmaceutical and / or CRO industries.Data Management experience and knowledge of CDISC standard are highly desirable.Good SAS programming skills and attention to detail are essential.Demonstrate knowledge of regulatory biostatistics, SOPs, and guidelines.Highly motivated and able to work well independently.Strong organizational, time management, communication and project coordination and leadership skills.Must be able to work well under timeline pressure.Must be able to work on multiple tasks while coordinating others at the same time.