General information
            
            
                
                
                
                
        
                
                
                    
                        Publication date
                    
                    13/02/2024
                
                
                
             Position description
	Category
OPERATIONS - CONSULTING
	Job title
Statistical Programmer M/F
	Contract
Permanent contract
	Contractual hours
Full time
	Job description
	- An experienced statistical programmer with a strong background in the Life
 Sciences industry.
- Skilled in data analysis , statistical modeling , and programming , with a proven
 track record of contributing to the successful execution of clinical trials and
 research projects.
- Committed to maintaining the highest standards of data quality , regulatory
 compliance , and efficiency in statistical programming.
- Provides statistical programming expertise to deliver high quality
- Develop Analysis Data Model (ADaM) datasets
- Develop (Tables, Figures and Listings (TFL)
 
 
- Output and Programming Specification [ OPS ]
 from the Statistical Analysis Plan [
 SAP ] or a related document
- Program and validate
- standard ADaM
- utility Statistical Analysis Software [ SAS ] macros or R function/package
 following good programming practices
 Statistical Programming: Proficient in SAS, R, and other statistical software.
 Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting.
 Data Management: Data validation, cleaning, and integration.
 Regulatory Compliance: Knowledge of FDA and EMA guidelines.
Programming Languages: SAS, R, Python.
 Statistical Analysis: Data modeling, hypothesis testing, and statistical inference.
 Data Visualization: Generating graphs, charts, and visual representations of data.
 Team Collaboration: Effective communication and teamwork in cross functional
environments.
 Problem Solving: Analyzing complex data challenges and finding innovative
solutions.
 
	Business Industry
Life sciences
	Profile
	Statistical Programming: Proficient in SAS, R, and other statistical software.
 Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting.
 Data Management: Data validation, cleaning, and integration.
 Regulatory Compliance: Knowledge of FDA and EMA guidelines.
Programming Languages: SAS, R, Python.
 Statistical Analysis: Data modeling, hypothesis testing, and statistical inference.
 Data Visualization: Generating graphs, charts, and visual representations of data.
 Team Collaboration: Effective communication and teamwork in cross functional
environments.
 Problem Solving: Analyzing complex data challenges and finding innovative
solutions.
 Position location
	Job location
Asia Pacific, India
	Location
	Bangalore
Candidate criteria
	Level of experience
All levels of experience
	Languages
English (4 : Native / Bilingual level)