Statistical Programming in Clinical Trials

Duration

3 Months, conducted on weekdays (Monday to Friday – 3 hours/day) And 3 Months, conducted on weekends (Saturday & Sunday- 5 hours/day)

Topics Covered

  • Base 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

Practical Training

Classroom practical training to demonstrate SAS® programming procedures, reporting, coding etc.

Tools Used

SAS® 9.4 License version software

Batch Size

10 students per batch

Eligibility

Candidates are preferred from

  • Life sciences (M.Pharm., B.Pharm., M.Sc.)
  • Statistics (B.Sc., M.Sc.)
  • BE /BTech (Biotechnology, Bioinformatics, Computer Science)
  • MBBS, BDS, BHMS, and BAMS

Features of this course

  • The program is specially designed by Cytel with its deep global expertise in biostatistics and clinical programming
  • We are offering substantial and quality Clinical Programming using SAS®
  • Trainers are experienced Clinical SAS® programmers with exposure to global clients including large Pharma and Biotech companies
  • The course covers the fundamentals of clinical operations
  • Practical exposure to SAS® 9.4 Programming with case studies
  • Datasets and examples related to the clinical trials domain
  • Regular assessments to improve and rank the performance
  • For batch schedule & course fee kindly contact us at respective locations or email us at [email protected]

Mode of Payment

  • Payment can be done by Cheque/DD/Credit Card/Debit Card/Online Transfer
  • Instalment facility available
  • Discounts available on full fees payments