Similar Jobs
See allContract Statistical Programmer
Iovance Biotherapeutics
Global
SAS
R
CDISC
Principal Data Scientist Consultant
ClinChoice
US
R
CDISC
SAS
Principal Statistician
Partner Company
US
Statistical Analysis
CDISC
SAS
Principal Biostatistician
Ergomed Group
Europe
Biostatistics
SAS
R
Senior/ Principal Statistical Programmer
Partner Company
India
R
SAS
SQL
Main Job Tasks and Responsibilities:
- Participate in CRF design, database review, data management plan, data review, and data validation procedures.
- Produce data listings, summary tables, and graphics for interim and final analyses.
- Integrate data across studies within a project and validate analysis datasets and TFLs from vendors.
Requirements:
- Minimum of 10 years of SAS programming in pharmaceutical or biotechnology industry with BA/BS in computer science, statistics, math, or MA/MS with 8 years.
- Expertise in SAS programming, report generation, and CDISC data standards required.
- Experience with Clinical Study Reports, NDA submission, and working in an FDA-regulated environment.
Who will you be working for?
- ClinChoice is a global full-service CRO with over 28 years of proven quality delivery.
- They emphasize a supportive culture, continuous training, and diversity and inclusivity across their workforce.
ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, they maintain a supportive culture focused on quality, professional development, and low turnover.