Online Training - Clinical SAS (Base SAS, Advance SAS and Biostatistics) with Project Experience Certification & Placement Assistance
BioMed Informatics Medwin Hospitals, Hyderabad, India is a leading Clinical Research Organization offering best SAS Training in Hyderabad since the year of 2000. Online SAS Training in Hyderabad, India includes best Clinical SAS Training online (Base SAS Programming course certification, Advance SAS Programming course certification and Biostatistics) to find out efficacy and safety of Investigational Product. BioMed Informatics Medwin Hospitals Online Training complimented as the best Clinical SAS Training in USA, best Clinical SAS Training in UK, best Clinical SAS Training in Australia, best Clinical SAS Training in Germany, best Clinical SAS Training in Sweden, best Clinical SAS Training in Netherlands, best Clinical SAS Training in Singapore, best Clinical SAS Training in Europe, best Clinical SAS Training in Canada. SAS (Statistical Analysis Software) was primarily developed by SAS Institute for the data management analysis. SAS Clinical Training online helps you gain the analytical skills to apply in Clinical studies. SAS Clinical online training course provides insights on developing the SAS programming to conduct analysis for the different types of clinical trials and new drug applications. With best Practical Hands on Live online Clinical SAS Programming Training, Analysts play predominant role in evaluation of drugs in clinical studies. Globally most of the Companies representing IT, Healthcare, Pharmaceutical, Biotechnology, SMO and Contract Research Organizations (CRO) have relied on SAS Programming to interpret the data. It is very difficult to draw a concrete conclusion from Clinical Research because of inherent differences between two individuals and also from group to group. The extent of this variability in a character is by way of chance, i.e., biological or normal is revealed by statistical methods. Interpretation, drawing conclusions and recommendations play a major role in Clinical Research.
SAS Certification Training
SAS Certification Training is intended to make you an expert in Base SAS Certification Training, Clinical SAS Certification Training, Advanced SAS Certification Training, SAS Clinical Certification Training, Biostatistics SAS Certification Training and Data analytics. SAS primarily comprises of Reading Data, Analysing Data and Reporting.
SAS Programming is used to find out Safety and Efficacy of Investigational Product (IP) in Clinical Research. SAS Programmers are required through the entire life cycle of a drug - starting at the preclinical development stage and going right through to continued monitoring of drugs once they hit the market.
If you're looking to boost your career prospects in the pharmaceutical industry, SAS training is a great string to add to your bow. Whether you want to move into clinical research or enhance your profile in your existing company, SAS training is crucial. Compliance to European and American Data regulations is important.
Brexit and implementation of the new regulatory base of Clinical Data in the UK, as well as in the Eurasian Economic Union (EAEU) countries, have transformed Clinical Data to a key element brought to the attention of all pharmaceutical industry players. For years, a globally harmonized approach to Clinical Data has been discussed as a concept for integrated regulations. Considering the recent developments, we are Getting Closer Harmonized systems.
SAS Certification Training Online
Looking for professional SAS Certification training ? If you hold an associate's degree or higher and want to advance your career in Clinical SAS, our Online Training - Clinical SAS (Base SAS, Advance SAS and Biostatistics) with Practical Hands on Training with Flexible Timings & Project Experience Certification with Placement Assistance is right for you to boost your career. Our SAS Certification training online focuses on ICH-GCP/FDA (US)/EMEA (Europe, the Middle East and Africa)/Canada (Health Canada)/TGA (Australia)/MHRA (UK) guidelines, and hands-on training. Unique program designed for professionals aspiring to make a career in Pharmaceutical industry using the in-demand, industry-based SAS Statistical Software.
Online Training Features
- Web based classroom
- One faculty/student
- Placement support
- Regular/Fast track/Weekend individual slot
- Flexible timings
- Training Mode: Skype/Teamviewer
Certification
Course Certificate & Job Experience Certificate would be awarded at the end of the program.
Course Curriculum
SAS Modules
- SAS / BASE
- SAS / STAT
- SAS / REPORT
- SAS / ODS
- SAS / GRAPH
- SAS / ACCESS
- SAS / CONNECT
- SAS / SQL
- SAS / MACROS
- LIVE SAS CLINICAL PROJECT
SAS BASE
- Introduction to SAS System & Architecture
- SAS Windowing Environment
- SAS Libraries
- Variables & SAS Syntax Rules
- Data Step and Proc Step
- Titles & Footnotes
- Proc Print Statement
- Proc Print Options
- Set Statement
- Dataset Options
- Options Statement
- Types of Input Statements
- Infile Statement With Options
- Keep, Drop and Rename Statements
- Update Statement
- Modify Statement
- Merging Concepts
- Interleaving Concept
- Logical Variables
- Retain Statement
- Formats and Informats
- Conditional Statements
- SAS Functions
- Do Statement
- Randomization
BASE SAS PROCEDURES
- Proc Sort
- Proc Append
- Proc Transpose
- Proc Contents
- Proc Format
- Proc Import
- Proc Export
- Proc Compare
- Proc Copy
- Proc Options
- Proc Forms
- Proc Datasets
- Proc Printto
- Proc Calendar
BIOSTATISTICS
- Introduction To Biostatistics - Clinical Applications
- Frequency Distribution Of Clinical data
- Clinical Data Presentation
- Measures Of Centering Constants
- Measures Of Dispersion
- Normal Distribution
- Null Hypothesis / Alternate Hypothesis
- p - Value Interpretation
- Sampling Variation
- Probability Concepts In Clinical Trials
- t-Test - Pharma Applications
- Chi Square test - Adverse Event Analysis
- Correlation & Regression - Estimation Analysis
- ANOVA - Efficacy Analysis
SAS / STAT (DATA ANALYSIS)
- Proc Means (mean, median, std, n, var, cv, range, q, q3, qrange, p50)
- Proc Univariate
- Proc Summary
- Proc TTest (Paired and Unpaired)
- Proc Anova (One Way, Two Way and Manova)
- Proc Glm
- Proc Freq
- Proc Chisq
- Proc Corr
- Proc Reg
SAS / GRAPH
- Proc Plot
- Proc Gplot
- Mutliple Plots & Overlay
- Symbol Statement
- Title and Footnote Statements
- Proc Chart
- Proc Gchart
- Vertical, Horizontal, Pie
- Group, Subgroups
- Proc G3D
- Proc Gprint
- Graph-N-Go
SAS / REPORT
- Proc Report
- Column Statements
- Break/Rbreak Statements
- Compute Statement
- Frequency Procedure
- Proc Tabulate
- One-Dimensional Tables
- Two-Dimensional Tables
- Summary Statistics
SAS / ODS
- ODS Statements
- ODS Options
- Using ODS to Create HTML, PDF, RTF
- Proc Template
- Proc Report with ODS
SAS / SQL
- Introduction to SAS/SQL
- Proc Sql Statements
- Proc Sql Options
- Set Clause
- Where Clause
- Order by Clause
- Group by Clause
- Having Clause
- Distinct Clause
- Formatting Output
- Case Expression and Conditional Logic
- Sql Set Operators
- Joins in Sql
- Creating ,Populating & Deleting Tables
- Alter Table Statement
- Renaming A Table & Columns
- Changing Column's Length
- Aggregate Functions
- Pass Through Facility
SAS / MACROS
- Macro Concepts
- Macros And Macro Variables
- Creating Macro Variables
- Using Macro Variables
- Invoking A Macro
- Passing Arguments to Macros
- Macro Quoting Functions
- Macro Options
- Macro Expressions
SAS / ACCESS
- Import & Export Procedures
- Proc Access
- Worksheet Statement
SAS / CONNECT
- Cimport Procedure
- Cport Procedure
- Using Select Statement
LIVE SAS CLINICAL PROJECT
You will be extensively involved in
- Extracting the data from various internal and external databases (Oracle, MS Access, Excel spreadsheets) using SAS/ACCESS, SAS/INPUT
- Developing programs for converting the Oracle data into SAS datasets using SQL Pass Through Facility
- Clinical trial data analysis with different Statistical Procedures
- Using various statistical procedures to find out the efficiency of the drug as per 21 CFR USFDA Guidelines
- Interpretation of p-value and drawing conclusions
- Assigning subjects to different treatment arms with SAS Randomization Programs
- Creating the reports using the SAS procedures and using ODS statements to generate different output formats like
- HTML, PDF, RTF and excel to view them in the web browser
- Creating the statistical reports using Proc Report, Proc Tabulate and SAS Macro
- Thorough understanding of Protocol, Statistical Analysis Plan (SAP)
- Analyzing the data and creating tables according to the Statistical Analysis Plan (SAP)
- Generating the demographic tables, adverse events and serious adverse events reports
- Using the SAS procedures (MEANS, FREQ, SUMMARY, TRANSPOSE, TABULATE, REPORT etc) and SAS/STAT procedures (REG, CORR, GLM, ANOVA and UNIVARIATE etc.) for summarization, cross-tabulations and statistical analysis
- Manipulation of SAS datasets using SET, MERGE, UPDATE, MODIFY and Conditional statements
- Generating Graphs and Figures using PROC CHART, PROC GCHART, PROC PLOT, PROC GPLOT and Graph-N-Go
- Validation and QC of the efficacy and safety tables
- Using PROC EXPORT and Export wizard to Transfer SAS data to external data sources
- Providing programming support for the creation and maintenance of programs used in Data Management, Data Validation, Data Cleaning and Statistical Report Generation
- Extensive Applications in SAS/SQL, SAS/ACCESS, SAS/CONNECT and SAS Macros
- Generating Tables, Listings, Figures/Graphs (TLFs or TLGs)
- Working with datasets such as DM (Demographics), LB (Laboratory), MH (Medical History), AE (Adverse Events), VS (Vital Signs), CM (Concomitant Medication)
- Manipulation and Reporting of clinical data using PROC SQL
- Extensive programming in writing and debugging the Macro routines and applying Macro variables in SAS program
- CDISC Standards (SDTM, ADaM, LAB, ODM)
- Live SAS Clinical Projects
Global SAS Data Regulations
Clinical SAS (Statistical Analysis System) programming is critical in the analysis, reporting, and submission of clinical trial data to regulatory agencies. While there are no specific "SAS regulations," its use in clinical trials is governed by broader Good Clinical Practice (GCP) guidelines, data integrity standards, and regulatory frameworks for clinical trial data. Below is an overview of the regulations affecting the use of Clinical SAS globally:
Oceania
Australia
- Agency: Therapeutic Goods Administration (TGA)
- Framework:
- Aligns with ICH E6 (R2) for GCP.
- Use of Clinical SAS must ensure data accuracy, traceability, and validation.
New Zealand
- Agency: MEDSAFE
- Framework:
- Requires compliance with ICH GCP standards for statistical programming.
North America
United States
- Agency: Food and Drug Administration (FDA)
- Framework:
- 21 CFR Part 11: Electronic records and signatures.
- FDA Guidance on Statistical Analysis.
Canada
- Agency: Health Canada
- Framework:
- Adheres to GCP and guidelines for statistical analysis in clinical trials.
Central/South America
Brazil
- Agency: ANVISA (AgenciaNacional de Vigilancia Sanitaria)
- Framework:
- Requires adherence to ICH GCP guidelines.
Mexico
- Agency: COFEPRIS
- Framework:
- Follows GCP.
Europe
European Union
- Agency: European Medicines Agency (EMA)
- Framework:
- Requires compliance with EMA statistical guidelines for clinical trials.
- Statistical programming tools like SAS must be validated and auditable.
United Kingdom
- Agency: Medicines and Healthcare Products Regulatory Agency (MHRA)
- Framework:
- Similar to EMA, emphasizes GCP.
Asia
India
- Agency: Central Drugs Standard Control Organization (CDSCO)
- Framework:
- Aligns with Schedule Y of the Drugs and Cosmetics Rules and ICH GCP.
- Validation of SAS programs for submissions.
China
- Agency: National Medical Products Administration (NMPA)
- Framework:
- Mandates compliance for clinical trial submissions.
- SAS programs must be validated for accuracy and reproducibility.
Japan
- Agency: Pharmaceuticals and Medical Devices Agency (PMDA)
- Framework:
- Enforces GCP for regulatory submissions.
- Validation of SAS programs is mandatory.
Middle East
Saudi Arabia
- Agency: Saudi Food and Drug Authority (SFDA)
- Framework:
- Follows ICH GCP standards.
United Arab Emirates
- Agency: Ministry of Health and Prevention (MOHAP)
- Framework:
- Aligns with ICH GCP for statistical analysis and programming.
Africa
South Africa
- Agency: South African Health Products Regulatory Authority (SAHPRA)
- Framework:
- Adheres to GCP.
Global Clinical SAS Salaries
Salaries for Clinical SAS (Statistical Analysis System) professionals vary globally depending on location, experience, and role within the pharmaceutical, biotech, or CRO sectors. Here's a general overview:
North America
USA
- Entry-level: $60,000-$80,000 per year
- Mid-level: $85,000-$120,000 per year
- Senior-level: $125,000-$180,000+ per year
Canada
- Entry-level: CAD 50,000-CAD 70,000 per year
- Mid-level: CAD 75,000-CAD 100,000 per year
- Senior-level: CAD 110,000-CAD 150,000+ per year
Europe
United Kingdom
- Entry-level: £25,000-£40,000 per year
- Mid-level: £45,000-£70,000 per year
- Senior-level: £75,000-£120,000+ per year
Germany/France/Netherlands
- Entry-level: €35,000-€50,000 per year
- Mid-level: €55,000-€80,000 per year
- Senior-level: €90,000-€140,000+ per year
Asia-Pacific
India
- Entry-level: ₹4,00,000-₹6,00,000 per year
- Mid-level: ₹7,00,000-₹12,00,000 per year
- Senior-level: ₹15,00,000-₹25,00,000+ per year
Japan
- Entry-level: ¥3,500,000- ¥5,000,000 per year
- Mid-level: ¥6,000,000- ¥10,000,000 per year
- Senior-level: ¥12,000,000- ¥18,000,000+ per year
Australia
- Entry-level: AUD 50,000-AUD 70,000 per year
- Mid-level: AUD 80,000-AUD 120,000 per year
- Senior-level: AUD 130,000-AUD 200,000+ per year
Middle East
UAE
- Entry-level: AED 120,000-AED 180,000 per year
- Mid-level: AED 200,000-AED 300,000 per year
- Senior-level: AED 350,000-AED 500,000+ per year
Saudi Arabia
- Entry-level: SAR 100,000-SAR 150,000 per year
- Mid-level: SAR 160,000-SAR 250,000 per year
- Senior-level: SAR 300,000-SAR 450,000+ per year
Africa
South Africa
- Entry-level: ZAR 300,000-ZAR 450,000 per year
- Mid-level: ZAR 500,000-ZAR 800,000 per year
- Senior-level: ZAR 1,000,000-ZAR 1,800,000+ per year
Nigeria/Kenya/Ghana
- Entry-level: $12,000-$20,000 per year
- Mid-level: $25,000-$40,000 per year
- Senior-level: $50,000-$80,000+ per year