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