Johnson & Johnson seeks an experienced statistical programmer to support clinical trial data analysis and reporting activities. The role involves designing and developing programs for clinical research, ensuring CDISC compliance, and collaborating with cross-functional teams on trials of low to medium complexity.
Responsibilities
Design and develop programs supporting clinical research analysis and reporting activities
Complete and lead programming trial activities with focus on quality and timely delivery of outputs
Verify programming and reporting activities; review project requirements and documentation
Create, verify, and deliver CDISC-compliant data packages and regulatory submission materials
Collaborate with programming team, data management, statistics, and clinical stakeholders on assigned projects
Requirements
Bachelor's degree in computer science, data science, mathematics, public health, or related scientific field
Approximately 2+ years of programming experience in pharmaceutical, CRO, biotech, or related industry
Proficiency in programming languages such as SAS, R, or Python for data manipulation and analysis
Basic knowledge of regulatory guidelines including ICH-GCP and clinical research concepts
Strong written and verbal communication skills
Familiarity with data structures and programming methods for statistical analysis
Johnson & Johnson seeks an experienced statistical programmer to support clinical trial data analysis and reporting activities. The role involves designing and developing programs for clinical research, ensuring CDISC compliance, and collaborating with cross-functional teams on trials of low to medium complexity. Responsibilities ...
Johnson & Johnson seeks an experienced statistical programmer to support clinical trial data analysis and reporting activities. The role involves designing and developing programs for clinical research, ensuring CDISC compliance, and collaborating with cross-functional teams on trials of low to medium complexity. Responsibilities ...
Senior Statistical Programmer 2 role at a global CRO involves leading programming initiatives, developing and validating clinical datasets using SAS, and providing consultancy on CDISC standards and regulatory submissions. The position requires mentoring team members and driving continuous improvement across biostatistical ...
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters.
Senior Statistical Programmer leading SAS programming for clinical trial data management and regulatory submissions. Develops CDISC datasets, mentors junior staff, and ensures compliance with regulatory standards across complex studies. Responsibilities - Develop, test, and execute SAS programs for CDISC-compliant datasets ...
... Computer Science, Data Analytics, or a related https://jobeax.com/link/nnF4EyWTLvU0XkJo and Technical Requirements :- Hands-on experience in SAS programming, statistical analysis, and data manipulation.- Proficiency in SAS Base, SAS Macro, and PROC SQL.- Experience in developing, testing, debugging, and maintaining SAS programs.- ...
... Computer Science, Data Analytics, or a related https://jobeax.com/link/nnF4EyWTLvU0XkJo and Technical Requirements :- Hands-on experience in SAS programming, statistical analysis, and data manipulation.- Proficiency in SAS Base, SAS Macro, and PROC SQL.- Experience in developing, testing, debugging, and maintaining SAS programs.- ...
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr. Statistical Programmer based in India . As a Senior Statistical Programmer, you will play a key role in transforming clinical trial data into accurate, meaningful statistical outputs that ...
... Computer Science, Data Analytics, or a related https://jobeax.com/link/nnF4EyWTLvU0XkJo and Technical Requirements :- Hands-on experience in SAS programming, statistical analysis, and data manipulation.- Proficiency in SAS Base, SAS Macro, and PROC SQL.- Experience in developing, testing, debugging, and maintaining SAS programs.- ...
... and Commercial organizations in Sanofi, globally. Main responsibilities: The Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, ...