Clinical SaS Programmar

Key Responsibilities & Requirements:

• 5+ years of hands-on experience in SDTM, ADaM, and TLF across various therapeutic areas and clinical trial phases.
• Strong experience in creating and delivering ADaM datasets and TLFs for clinical trial studies.
• Proficient in creating and working with utility macros to support programming tasks.
• Skilled in creating specifications for datasets and deliverables.
• Familiarity with CDISC standards, including CDASH, SDTM, and ADaM.
• Ability to work independently as well as collaboratively within a team environment.
• Open to learning new tools and technologies and sharing knowledge with team members.
• Strong communication skills – written, verbal, interpersonal, and organizational.
• Proficient in SAS Enterprise Guide (EG) and SAS Studio for programming.
• Comfortable working in a Unix environment and using Unix-based tools.
• Prior experience in vaccines or oncology studies is an added advantage.
• Familiar with statistical procedures/functions used to create Tables, Listings, and Figures (TLFs).