Senior Statistical Programmer (RWE- Real World Evidence)
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 Statistical Programmer-RWE to join one of our clients.
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.
The Senior Statistical Programmer provides technical guidance on clinical and real-world evidence (RWE) project teams. Work is performed on the design, development, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical and real-world data (RWD) for individual studies. In addition, the Senior Statistical Programmer participates in departmental and cross-functional technology development and process improvement initiatives.
Key Duties and Responsibilities:
• Codes complex SAS programs (including Macro language, SAS/STAT, and SAS/GRAPH) for applications designed to analyze and report complex clinical and real-world data, ensuring high-quality deliverables.
• Develops and maintains SAS programs for the integration, transformation, and standardization of RWD, including claims, electronic health records (EHR), and registry data.
• Performs quality control checks of SAS code and output produced by other Statistical Programmers.
• Demonstrates proficient knowledge of clinical development, real-world data sources, and medical data interpretation.
• Solves clinical and RWE reporting problems and has proven technical proficiency in supporting daily operations, ensuring project tasks are completed accurately with limited supervision.
• Creates CDISC datasets, including SDTM and ADaM, by transforming various raw data sources, such as Electronic Data Capture (EDC) databases, Interactive Web Response Systems (IWRS), claims data, EHR, and registries.
• Works with all types of coding dictionaries (MedDRA and WHODD) commonly used in clinical and real-world evidence analysis.
• Provides technical leadership in a team environment, solving clinical and RWE reporting challenges within budget and customary timeline constraints while assuring high-quality standards.
Knowledge and Skills:
• Strong competence with SAS and experience with RWD programming.
• Working knowledge of CDISC Standards, including SDTM, ADaM, and real-world data transformation techniques.
• Familiarity with common RWE data sources such as claims, EHR, registries, and other observational datasets.
• Knowledge of real-world study methodologies, epidemiological study designs, and statistical approaches in RWE analysis.
• Effective communication (written and verbal) skills to exchange complex information with cross-functional teams.
Education and Experience:
• Bachelor's/Master's degree in a Scientific Discipline.
• Typically requires 5+ years for M.S. or above and 7+ years for B.S. of work experience in Biotech, Pharmaceuticals, or CRO, with a strong focus on RWE and clinical programming.
• Experience working with large observational databases is preferred.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for 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 is the core instrument 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 below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#Senior #Contract
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 Statistical Programmer-RWE to join one of our clients.
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.
The Senior Statistical Programmer provides technical guidance on clinical and real-world evidence (RWE) project teams. Work is performed on the design, development, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical and real-world data (RWD) for individual studies. In addition, the Senior Statistical Programmer participates in departmental and cross-functional technology development and process improvement initiatives.
Key Duties and Responsibilities:
• Codes complex SAS programs (including Macro language, SAS/STAT, and SAS/GRAPH) for applications designed to analyze and report complex clinical and real-world data, ensuring high-quality deliverables.
• Develops and maintains SAS programs for the integration, transformation, and standardization of RWD, including claims, electronic health records (EHR), and registry data.
• Performs quality control checks of SAS code and output produced by other Statistical Programmers.
• Demonstrates proficient knowledge of clinical development, real-world data sources, and medical data interpretation.
• Solves clinical and RWE reporting problems and has proven technical proficiency in supporting daily operations, ensuring project tasks are completed accurately with limited supervision.
• Creates CDISC datasets, including SDTM and ADaM, by transforming various raw data sources, such as Electronic Data Capture (EDC) databases, Interactive Web Response Systems (IWRS), claims data, EHR, and registries.
• Works with all types of coding dictionaries (MedDRA and WHODD) commonly used in clinical and real-world evidence analysis.
• Provides technical leadership in a team environment, solving clinical and RWE reporting challenges within budget and customary timeline constraints while assuring high-quality standards.
Knowledge and Skills:
• Strong competence with SAS and experience with RWD programming.
• Working knowledge of CDISC Standards, including SDTM, ADaM, and real-world data transformation techniques.
• Familiarity with common RWE data sources such as claims, EHR, registries, and other observational datasets.
• Knowledge of real-world study methodologies, epidemiological study designs, and statistical approaches in RWE analysis.
• Effective communication (written and verbal) skills to exchange complex information with cross-functional teams.
Education and Experience:
• Bachelor's/Master's degree in a Scientific Discipline.
• Typically requires 5+ years for M.S. or above and 7+ years for B.S. of work experience in Biotech, Pharmaceuticals, or CRO, with a strong focus on RWE and clinical programming.
• Experience working with large observational databases is preferred.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for 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 is the core instrument 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 below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#Senior #Contract
