Statistical Programmer (Remote)
A biotech company in North Carolina is seeking a new Statistical Programmer to join their team remotely, developing SAS programming deliverables for clinical study analysis and reporting.
• **This is a Remote opportunity.***
Responsibilities:
• Programming and validating tables, listings, figures, and derived datasets using SAS
• Developing SDTM and ADaM datasets and supporting documentation
• Preparing and reviewing mapping specifications and annotated case report forms (CRFs)
• Performing quality control and validation activities for programming deliverables
• Collaborating with study team members to resolve data and output issues
• Performing other duties, as needed
Qualifications:
• Minimum of 10 years of relevant Statistical Programming experience
• Bachelor's Degree
• Strong skills in SAS programming
• Experience developing SDTM, ADaM, tables, listings, and figures.
• Strong knowledge of Clinical Trial processes, Regulatory requirements, and Programming Documentation
• Strong analytical and problem-solving skills
• Excellent communication skills
• Strong attention to detail
Desired Qualifications:
• Master's Degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.
• Phase 3 and Regulatory Submission experience
Apply tot his job
Apply To this Job
• **This is a Remote opportunity.***
Responsibilities:
• Programming and validating tables, listings, figures, and derived datasets using SAS
• Developing SDTM and ADaM datasets and supporting documentation
• Preparing and reviewing mapping specifications and annotated case report forms (CRFs)
• Performing quality control and validation activities for programming deliverables
• Collaborating with study team members to resolve data and output issues
• Performing other duties, as needed
Qualifications:
• Minimum of 10 years of relevant Statistical Programming experience
• Bachelor's Degree
• Strong skills in SAS programming
• Experience developing SDTM, ADaM, tables, listings, and figures.
• Strong knowledge of Clinical Trial processes, Regulatory requirements, and Programming Documentation
• Strong analytical and problem-solving skills
• Excellent communication skills
• Strong attention to detail
Desired Qualifications:
• Master's Degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.
• Phase 3 and Regulatory Submission experience
Apply tot his job
Apply To this Job