A clinical research organization is looking for a Statistical Programmer in Jacksonville, Florida. The ideal candidate will have expertise in SAS programming and statistical reporting, with a requirement of a Master's degree and at least 3 years of experience or a Bachelor's with 5 years. Responsibilities include designing SAS programs for clinical trials, validating datasets, and collaborating with interdisciplinary teams to ensure quality and compliance. Strong problem-solving and communication skills are essential for this role.
Qualifications
Minimum of 3 years of experience with an MS or 5 years with a BS in related fields.
Experience supporting early and late phase clinical trials.
Excellent skills in SAS programming and reporting.
Knowledge of CDISC standards and FDA submission requirements.
Familiarity with FDA and ICH regulations.
Responsibilities
Design and code SAS programs for clinical projects.
Deliver CDISC compliant SDTM and ADaM datasets.
Create and validate tables, figures, and listings.
Perform quality control checks and validation of SAS code.
Review or author eCRF, SDTM, and ADaM dataset specifications.
Skills
SAS programming
Statistical reporting
Problem-solving
Communication skills
Education
MS in Statistics, Computer Science, or related field
BS in Statistics, Computer Science, or related field
Job description
A clinical research organization is looking for a Statistical Programmer in Jacksonville, Florida. The ideal candidate will have expertise in SAS programming and statistical reporting, with a requirement of a Master's degree and at least 3 years of experience or a Bachelor's with 5 years. Responsibilities include designing SAS programs for clinical trials, validating datasets, and collaborating with interdisciplinary teams to ensure quality and compliance. Strong problem-solving and communication skills are essential for this role.