Job Title: Senior SAS Analyst / Statistical Programmer (ADaM)
Location: Chicago Ridge IL / 100% Remote
Type: Contract
Job Summary
We are seeking an experienced Senior SAS Analyst / Statistical Programmer with strong expertise in ADaM SDTM and regulatory submissions. This role involves leading programming activities managing a team of statistical programmers and delivering high-quality outputs aligned with regulatory standards.
The ideal candidate will have extensive experience in clinical trial data programming including integrated analyses and regulatory filings preferably within therapeutic areas such as oncology neuroscience or immunology.
Key Responsibilities
- Lead and manage a team of Statistical Programmers
- Develop and review ADaM datasets TFLs (Tables Listings Figures) and SDTM datasets
- Ensure timely delivery of high-quality outputs in compliance with regulatory requirements
- Support regulatory submissions (eSubmissions) and integrated analyses
- Mentor and train junior team members
- Collaborate with cross-functional teams including Biostatistics and Clinical Data Management
- Maintain documentation and ensure adherence to industry standards and best practices
Required Qualifications
- Bachelors or Masters degree in Statistics Computer Science or related field
- 10 years of experience in SAS programming within clinical trials
- Strong expertise in ADaM SDTM TFLs and eSubmissions
- Experience in integrated analysis and regulatory filings
- Proven experience in team leadership and project management
- Excellent communication and problem-solving skills
Job Title: Senior SAS Analyst / Statistical Programmer (ADaM) Location: Chicago Ridge IL / 100% Remote Type: Contract Job Summary We are seeking an experienced Senior SAS Analyst / Statistical Programmer with strong expertise in ADaM SDTM and regulatory submissions. This role involves leading pro...
Job Title: Senior SAS Analyst / Statistical Programmer (ADaM)
Location: Chicago Ridge IL / 100% Remote
Type: Contract
Job Summary
We are seeking an experienced Senior SAS Analyst / Statistical Programmer with strong expertise in ADaM SDTM and regulatory submissions. This role involves leading programming activities managing a team of statistical programmers and delivering high-quality outputs aligned with regulatory standards.
The ideal candidate will have extensive experience in clinical trial data programming including integrated analyses and regulatory filings preferably within therapeutic areas such as oncology neuroscience or immunology.
Key Responsibilities
- Lead and manage a team of Statistical Programmers
- Develop and review ADaM datasets TFLs (Tables Listings Figures) and SDTM datasets
- Ensure timely delivery of high-quality outputs in compliance with regulatory requirements
- Support regulatory submissions (eSubmissions) and integrated analyses
- Mentor and train junior team members
- Collaborate with cross-functional teams including Biostatistics and Clinical Data Management
- Maintain documentation and ensure adherence to industry standards and best practices
Required Qualifications
- Bachelors or Masters degree in Statistics Computer Science or related field
- 10 years of experience in SAS programming within clinical trials
- Strong expertise in ADaM SDTM TFLs and eSubmissions
- Experience in integrated analysis and regulatory filings
- Proven experience in team leadership and project management
- Excellent communication and problem-solving skills
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