Senior Clinical SAS Macro Developer
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...
ClinChoice is searching for a Senior Clinical SAS Macro Developer Consultant to join one of our clients.
The Clinical SAS Macro Programmer will have strong experience in CDISC standards (SDTM, ADaM) and clinical trial data. You will be responsible for designing, developing, and maintaining robust and reusable SAS macros to support automation and ensure quality control across statistical programming deliverables.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Main Job Tasks and Responsibilities:
Design, develop, and validate SAS macros to streamline clinical trial programming workflows, reduce manual effort, and improve consistency and compliance.
Collaborate with biostatisticians, clinical programmers, and data managers to gather requirements and implement solutions aligned with CDISC standards.
Develop QC tools and utilities to automate validation and ensure regulatory compliance (e.g., FDA submissions).
Create documentation for macros, including user guides, validation plans, and test cases, following industry best practices.
Support the deployment and maintenance of macro libraries across studies and therapeutic areas.
Troubleshoot, optimize, and enhance existing macros and tools.
Ensure adherence to Good Programming Practices (GPP) and regulatory standards, including ICH, FDA, and CDISC guidelines.
Requirements:
Bachelor’s or Master’s degree in Computer Science, Statistics, Life Sciences, or a related field.
5+ years of SAS programming experience in the clinical trials or pharmaceutical industry.
Proven experience in macro development using Base SAS and SAS Macro Language.
Strong working knowledge of CDISC SDTM and ADaM standards.
Experience with clinical trial data structures and regulatory submission requirements.
Familiarity with validation and quality control procedures in clinical programming.
Excellent problem-solving and communication skills.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we have received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training are the core instruments to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our low industry-average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent, guided by a commitment to diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#LI-#TT1 #LI-Remote #Senior#Contract
Senior Clinical SAS Macro Developer
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...
ClinChoice is searching for a Senior Clinical SAS Macro Developer Consultant to join one of our clients.
The Clinical SAS Macro Programmer will have strong experience in CDISC standards (SDTM, ADaM) and clinical trial data. You will be responsible for designing, developing, and maintaining robust and reusable SAS macros to support automation and ensure quality control across statistical programming deliverables.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Main Job Tasks and Responsibilities:
Design, develop, and validate SAS macros to streamline clinical trial programming workflows, reduce manual effort, and improve consistency and compliance.
Collaborate with biostatisticians, clinical programmers, and data managers to gather requirements and implement solutions aligned with CDISC standards.
Develop QC tools and utilities to automate validation and ensure regulatory compliance (e.g., FDA submissions).
Create documentation for macros, including user guides, validation plans, and test cases, following industry best practices.
Support the deployment and maintenance of macro libraries across studies and therapeutic areas.
Troubleshoot, optimize, and enhance existing macros and tools.
Ensure adherence to Good Programming Practices (GPP) and regulatory standards, including ICH, FDA, and CDISC guidelines.
Requirements:
Bachelor’s or Master’s degree in Computer Science, Statistics, Life Sciences, or a related field.
5+ years of SAS programming experience in the clinical trials or pharmaceutical industry.
Proven experience in macro development using Base SAS and SAS Macro Language.
Strong working knowledge of CDISC SDTM and ADaM standards.
Experience with clinical trial data structures and regulatory submission requirements.
Familiarity with validation and quality control procedures in clinical programming.
Excellent problem-solving and communication skills.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we have received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training are the core instruments to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our low industry-average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent, guided by a commitment to diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#LI-#TT1 #LI-Remote #Senior#Contract