Statistical Programmer (Remote)
Posted 7 days ago by Tandym Tech
Negotiable
Undetermined
Remote
Remote
Summary: A biotech company in North Carolina is looking for a Statistical Programmer to work remotely, focusing on SAS programming deliverables for clinical study analysis and reporting. The role requires extensive experience in statistical programming and collaboration with study teams to ensure data integrity and compliance with regulatory standards. The position emphasizes the development of datasets and documentation essential for clinical trials. Candidates should possess strong analytical skills and attention to detail.
Key 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
Key Skills:
- 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
Salary (Rate): undetermined
City: undetermined
Country: undetermined
Working Arrangements: remote
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
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