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Get Brochure to Your MailIndia's Top Rated Clinical SAS training for Pharma/ Biotech/Life Science/Clinical Research graduates. Learn how to use Clinical SAS, from beginner basics to advanced techniques, with Best Clinical SAS Training institutes taught by industry experts. Clin Infotech offer unique and customized job-oriented real-world data Clinical SAS Course.
Our Projects
During the SAS internship period you working on the Projects
Hands On Experience on Real Time Projects
Our Internship Confined with the complete hands on experience on Real Time Projects. Classroom practical training to demonstrate SAS programming procedures, reporting, coding etc…
Clinical SAS Internship Duration and Timing
At Clin InfoTech’s, we offer 6 Months Internship Program for your convenience.
We also offer fast track classes to meet your busy schedule.
SAS Internship Benefits
- Training curriculum is specially designed by SAS Institute with its deep global expertise in biostatistics and clinical programming
- We are offering substantial and quality Clinical SAS® Training
- Trainers are experienced Clinical SAS® programmers with exposure to global clients including large Pharma and Biotech companies
- Course covers fundamentals of clinical operations
- Practical exposure to SAS® Programming with case studies
- Datasets and examples related to clinical trials domain
- Regular assessments to improve and rank the performance
- Soft skills training to facilitate placements
- In-house recruitment and placement assistance
Our SAS Internship Modules
- Clinical Programming Using SAS® 9.4 Training Syllabus
- Basic SAS®
- SAS® Macros
- SAS® SQL
- SAS® Graphs
- Introduction to clinical research and terminologies in clinical research
- Phases of clinical trials & drug development process
- Principles of GCP and Schedule Y
- Regulatory and ethical guidelines in clinical research
- Informed consent – Elements and documentation
- Clinical Trial – Key Documents
- Introduction to CDISC, SDTM & ADaM
- 10 Clinical Case Studies
Clinical Trials Process
- Describe the clinical research process (phases, key roles, key organizations).
- Interpret a Statistical Analysis Plan.
- Derive programming requirements from an SAP and an annotated Case Report Form.
- Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices).
Clinical Trials Data Structures
- Identify the classes of clinical trials data (demographic, lab, baseline, concomitant medication, etc.).
- Identify key CDISC principals and terms.
- Describe the structure and purpose of the CDISC SDTM data model.
- Describe the structure and purpose of the CDISC ADaM data model.
- Describe the contents and purpose of define.xml.
Import and Export Clinical Trials Data
- Combine SAS data sets.
- Efficiently import and subset SAS data sets.
- Access data in an Excel workbook (LIBNAME and PROC IMPORT/EXPORT).
- Create temporary and permanent SAS data sets.
- Apply regulatory requirements to exported SAS data sets (SAS V5 requirements).
Manage Clinical Trials Data
- Investigate SAS data libraries using base SAS utility procedures (PRINT, CONTENTS, FREQ).
- Access DICTIONARY Tables using the SQL procedure.
- Sort observations in a SAS data set.
- Create and modify variable attributes using options and statements in the DATA step.
- Examine and explore clinical trials input data (find outliers, missing vs. zero values, etc).
Transform Clinical Trials Data
- Process data using DO LOOPS.
- Process data using SAS arrays.
- Retain variables across observations.
- Use assignment statements in the DATA step.
- Apply categorization and windowing techniques to clinical trials data.
- Use SAS functions to convert character data to numeric and vice versa.
- Use SAS functions to manipulate character data, numeric data, and SAS date values.
- Transpose SAS data sets.
- Apply 'observation carry forward' techniques to clinical trials data (LOCF, BOCF, WOCF).
- Calculate 'change from baseline' results.
- Obtain counts of events in clinical trials.
Apply Statistical Procedures for Clinical Trials
- Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, SUMMARY).
- Use PROC FREQ to obtain p-values for categorical data (2x2 and NxP test for association).
- Use PROC TTEST to obtain p-values for continuous data (one-sample, paired and two-sample t-tests).
- Create output data sets from statistical procedures.
Macro Programming for Clinical Trials
- Create and use user-defined and automatic macro variables.
- Automate programs by defining and calling macros.
- Use system options to debug macros and display values of macro variables in the SAS log (MPRINT, SYMBOLGEN, MLOGIC, MACROGEN).
Report Clinical Trials Results
- Use PROC REPORT to produce tables and listings for clinical trials reports.
- Use ODS and global statements to produce and augment clinical trials reports.
Validate Clinical Trial Data Reporting
- Explain the principles of programming validation in the clinical trial industry.
- Utilize the log file to validate clinical trial data reporting.
- Use programming techniques to validate clinical trial data reporting (PROC COMPARE, MSGLEVEL).
- Identify and resolve data, syntax and logic errors.
Clinical SAS Training & Placement
Since 2011 over 1500 students have been placed in various analytics companies from niche startups to large multinationals.
Clin Infotech helps companies hire certified and trained candidates in SAS, Clinical & Life Sciences, Consulting, Market Analysis, and Business Analysis domains.
Clinical SAS Training Course Highlights:
- Two days free trial - If candidate likes this course, these days are adjusted in the schedule.
- Live project exposure of Fortune companies.
- Training by experts from CMM Level 5 companies.
- Worldwide classroom and corporate training at affordable fees.
- Basic course worth more than advanced courses of others.
- Free interview preparation and 100% assistance with certifications.
- Also offer training for foreign students.
Key Differentiators at Clin Infotech
- Courses designed by experts with 25+ years of experience.
- Real-world experienced statistical programmers as faculty.
- Learn to handle real scenarios like imperfect data and unclear specs.
- Training includes project communication, specs, QC, and more.
- Industry-recognized certificate and interview grooming included.
- Authorized and licensed software used.
Clinical SAS Training Duration
- Weekday / Weekend classes available.
- Fast track (1-on-1) options for flexible hours.
About The Trainer
Our Trainer work as an SAS Consultant & Instructor, And has over 15 years of SAS Implementation experience and recognized expert in as a statistician in a large pharmaceutical company. Our Trainer specializes in SAS® programming in Clinical Trials. – They also been as Senior Instructor of SAS Institute and provided 150 Corporate trainings, trained 1500 corporate & fresher employees.
He is among few of the Certified SAS programmer in the World to achieve below certifications in his area of research.
- SAS Certified Base Programmer for SAS 9
- SAS Certified Advanced Programmer for SAS 9
- SAS Certified Clinical Trials Programmer Using SAS 9
- SAS Certified Data Scientist Using SAS 9
- SAS Certified Advanced Analytics Professional Using SAS 9
- SAS Certified Predictive Modeler Using SAS Enterprise Miner 14
- SAS Certified Statistical Business Analyst Using SAS 9
- SAS Certified BI Content Developer for SAS 9
- SAS Certified Visual Business Analyst
- SAS Certified Visual Modeler Using SAS Visual Statistics 7.4
- SAS Certified Big Data Professional Using SAS 9
- SAS Certified Data Integration Developer for SAS 9
- SAS Certified Data Quality Steward for SAS 9
- SAS Certified Platform Administrator for SAS 9
Why CLIN INFOTECH?
- Clin Infotech is a leading training institute in the field of Advance Clinical Research Training Program. Here's why you should choose us:
- Industry-Experienced Faculty: Our instructors are seasoned professionals with extensive industry experience, ensuring that you receive practical insights and real-world perspectives.
- Hands-on Approach: We emphasize a hands-on learning approach, enabling you to apply theoretical concepts to practical scenarios.
- Customized Learning Paths: Our programs are designed to cater to learners of various backgrounds and skill levels, allowing you to learn at your own space.
- Job Placement Assistance: We provide comprehensive job placement assistance to help you secure lucrative career opportunities in the IT industry.
- Our Alumni Work At:
- Our alumni have successfully secured positions in leading organizations. Their achievements reflect the quality of our training programs and the practical skills they gained during their time with us.
Eligibility:
Minimum Eligibility Criteria For Application To The Course Would Be Either Of The Following:
Applicants are recommended to have one of the following life Science degrees: Bachelor’s, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / M.Tech (Biotechnology), B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) and all professionals working with Pharmaceutical companies, CROs and Hospital.
Admission Process:
The admission process for the Medical Writing Course with 100% placement assistance is very simple. Candidates can apply online through our website. After examining your application our executives contact you to complete the further procedure.
At Clin Infotech Systems, we are committed to assisting you every step of the way with our user-friendly online application process and committed admission officers. Prepare yourself to begin a fulfilling career in Medical Writing with our thorough admissions procedure.
Step 1: Apply Online at https://www.clininfotech.com
Step 2: Review the Application
Step 3: Contact and Further Process
Step 4: Enrolment and Confirmation
Step 5: Course Completion
Step 6: Assessments and Assignments
Step 7: Mock Test and Mock Interview
Step 8: Resume Preparation
Step 9: Skill Development
Step 10: Placement Assistance
Trainers and Training Process
At Clin Infotech, we have the best faculties with 15+ years of real-time experience in the clinical research industry. The course curriculum is specially developed with respect to the current industry trends and standards. Students will have the access to our online sessions. Additionally, the students will get a chance to clear their doubts on alternate weekends. Also, the practice interview sessions are also conducted by our trainers followed by timely assessments.
The trainers will help our students to pass their interviews smoothly and get placed in a good company.
Clin Infotech ADVANTAGE:
- Complete Course Material will be provided including detailed information about the entire workflow of a Clinical Research Associate.
- 2 months internship available after rigorous training in Medical Writing.
- Own CRO live projects.
- Highest placement record across all training institutes.
- Industry-based SOPs training.
- Trainers with a minimum of 7+ years of experience.
- Comprehensive teaching by medical doctors.
- Hands-on training will be provided on clinical research sites.
Our team of experienced drug safety specialists also provides the following services upon successful completion of the training:
- Resume Preparation
- Interview Preparation with real-time questions and answers
- Mock Interview Sessions
- Communication Skills and Personality Development Sessions
- Placement Assistance
- Placement Assurance
It's time to comprehend and put standard trail management ideas into practice in order to build a solid methodology for the evaluation and boost the timely completion of crucial trials for the benefit of patients. To plan, produce, monitor, and complete all project duties, you must acquire specific skills and knowledge.
Through its comprehensive certification program, Clin Infotech offers thorough instruction in clinical research throughout the whole clinical trial process. With the help of this clinical trial management course, instructors will make sure that students have a procedural and administrative understanding of the clinical trial process as well as the capacity to advance their knowledge and abilities.
This curriculum will teach you the whole Regulatory responsibilities involved in Document Creation; Planning, Organizing, Monitoring, Recording, Analysis, and Reporting of Human Clinical Trials, as well as the most recent discoveries and specialties in e-Clinical Technology.