Senior Real-World Evidence (RWE) Analyst / Programmer
ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Senior Real-World Evidence (RWE) Analyst/Programmer on a permanent basis.
Join our team: you can be part of making a difference in people’s lives and experience a fulfilling and rewarding career!
Main Job Tasks and Responsibilities:
Design and execute statistical programming to support real-world evidence studies.
Work with observational datasets such as claims, EHR, and registries.
Apply appropriate statistical methodologies (e.g., propensity score matching, regression modeling, survival analysis).
Develop, validate, and maintain reusable SAS and R macros or functions.
Collaborate with epidemiologists, statisticians, and HEOR experts on study design and data interpretation.
Contribute to protocol development, statistical analysis plans (SAPs), and final reports or publications.
Ensure compliance with data governance, privacy (e.g., HIPAA), and company policies
Requirements:
Bachelor’s or Master’s degree in Biostatistics, Statistics, Epidemiology, Computer Science, or a related field.
5+ years of experience in statistical programming within life sciences, with at least 3 years in RWE or observational research.
Strong programming experience in SAS and R.
Hands-on experience with real-world data sources (e.g., MarketScan, Optum, Flatiron, IQVIA, Cerner).
Strong knowledge of epidemiologic and statistical methods used in observational research.
Experience with regression models, survival analysis, propensity score techniques, etc.
Ability to interpret results and generate insights that are meaningful to cross-functional teams.
Excellent communication skills and ability to work independently.
Preferred Qualifications
Familiarity with clinical trial data and integration with RWD.
Knowledge of data visualization in R (ggplot2, Shiny, etc.).
Experience working in pharma/biotech or CRO setting.
Understanding of FDA and EMA guidelines on RWE.
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 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 #FTE
Senior Real-World Evidence (RWE) Analyst / Programmer
ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Senior Real-World Evidence (RWE) Analyst/Programmer on a permanent basis.
Join our team: you can be part of making a difference in people’s lives and experience a fulfilling and rewarding career!
Main Job Tasks and Responsibilities:
Design and execute statistical programming to support real-world evidence studies.
Work with observational datasets such as claims, EHR, and registries.
Apply appropriate statistical methodologies (e.g., propensity score matching, regression modeling, survival analysis).
Develop, validate, and maintain reusable SAS and R macros or functions.
Collaborate with epidemiologists, statisticians, and HEOR experts on study design and data interpretation.
Contribute to protocol development, statistical analysis plans (SAPs), and final reports or publications.
Ensure compliance with data governance, privacy (e.g., HIPAA), and company policies
Requirements:
Bachelor’s or Master’s degree in Biostatistics, Statistics, Epidemiology, Computer Science, or a related field.
5+ years of experience in statistical programming within life sciences, with at least 3 years in RWE or observational research.
Strong programming experience in SAS and R.
Hands-on experience with real-world data sources (e.g., MarketScan, Optum, Flatiron, IQVIA, Cerner).
Strong knowledge of epidemiologic and statistical methods used in observational research.
Experience with regression models, survival analysis, propensity score techniques, etc.
Ability to interpret results and generate insights that are meaningful to cross-functional teams.
Excellent communication skills and ability to work independently.
Preferred Qualifications
Familiarity with clinical trial data and integration with RWD.
Knowledge of data visualization in R (ggplot2, Shiny, etc.).
Experience working in pharma/biotech or CRO setting.
Understanding of FDA and EMA guidelines on RWE.
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 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 #FTE