Training as Internship
ID# :Q-IN-2017-PS049
Date Posted : 08-11-2017 (mm-dd-yyyy)
Title : Clinical SAS Programmer

Classification: Training program as Internship

Location: On-Site
Contact:
Director Operations
Qtech Solutions Inc.
3 Executive Drive, Suite 320
Somerset, New Jersey USA 08873
Phone : 732-770-4100 Fax: 888-532-0210
Email :  hrs@qtech-solutions.com

Training Program

Qtech-Sol Training division doing business as Qtech-Sol Professional Development Center (QPDC) is a Private Vocational School and its Clinical Science programs are approved by New Jersey State - Department of Education and New Jersey Department of Labor and Workforce Development. We primarily engage in offering an array of short duration certificate courses for corporate, professionals and students. Our CDOT Package program offered, allows you to focus on securing a career advancement job.

Clinical Data Oriented Program (CDOT)

  1. Clinical SAS Programmer Program - 45 Days
  2. Post Training Assistance (Resume Prep, Narratives, and Mock Session) - 15 Days
  3. SAS Basic and Advanced Certification is a plus.
    The Candidate must know SAS Basics and Advanced to participate in CDOT Program.
    The Candidate must have SAS Software to Practice during this program.

This program allows you to better place your profile with clients for possible jobs. The job market requires experience and understanding of Clinical Trial Domain and SAS to perform various tasks for statistical data analysis and reporting. Qtech-Sol package program, will provide the required experience to jump-start.

This Training Program as Internship provides students hands-on about the various tasks and duties performed by Clinical SAS Programmer / Statistical Programmer to work at Pharmaceuticals, Hospitals and Research organizations towards clinical trial process across various phases. This Training program is Unpaid Internship and is conducted for 6 Weeks to Fresh and Alumni Students. Selection of Student is based on education background and GPA, subject to Interview performance. Student will participate into this program remotely. Students attending the Training program as Internship must plan to attend to spend minimum 4 hours/ day to submit the deliverables per schedule. The lessons will educate the student on the CDOT task to perform, client settings followed in Industry, team-work and submit timely the allocated deliverable tasks as part of this learning. During this Training Program, the candidate will have access to Qtech Proprietary forms, data and related presentations. The Student will be exposed to various CDOT Job related hypothetical tasks to gain required experience. The tasks are evaluated and feedback is provided via email. Candidates who have successfully completed the program will be provided a certificate of completion. Candidate who cannot participate on-site, can participate from their home as virtual-Internship.

Learning’s Gained during this Training Program

  • Elementary SAS Concepts
  • SAS Efficiency Programming
  • Introduction to Clinical Trials
  • Types and Data in Clinical Trials
  • Clinical Trial Protocol Development
  • Elements of CRF Design
  • Electronic Data Capture (EDC)
  • Good Clinical Practices
  • Good Documentation Practices
  • Work Flow Instruction Request
  • Documentation Templates
  • Introduction to Data Validation
  • Data Based Validation
  • Protocol Based Validation
  • Basic of Statistics
  • Statistical Analysis Planning
  • Elements of Hypothesis Testing
  • Basic of Efficiency
  • Integrated Summary of Effectiveness (ISE)
  • Integrated Summary of Safety (ISS)
  • Clinical Data Interchange Standards Consortium
  • Preparing Analysis Data sets
  • Creating Tables Listing and Graphs (TLG)
  • Understanding Various Therapeutics Areas
  • Data Based Therapy
  • Introduction to Phase I Studies
  • Oncology Project
  • Introduction to Phase II Studies
  • Ophthalmology Project
  • Introduction to Phase III Studies
  • Cardiology Project
  • Introduction to Phase IV Studies
  • Central Nervous Systems (CNS) Project
  • Introduction to Pharmacovigilance
  • Pharmacovigilance Reporting
  • Aggregate Reporting Process (PSUR, PUR, ADR, Signaling, etc.)
  • PSUR
 
Education : Bachelors / Master’s Degree in:
Biostatistics, Statistics, Biotechnology, Economics, Information Technology, Computer Science, Applied Mathematics, and Engineering (IT).
 
Experience : 0 years
 
Application End Date: 11-30-2017 (mm-dd-yy)
 

Please forward Your resumes along with ID to hrs@qtech-solutions.com

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