Sharija Peethambaran

Clinical SAS Team Lead with extensive experience in clinical data analysis, statistical programming, and regulatory submissions within the pharmaceutical and healthcare industry. Skilled in SAS programming, CDISC standards (SDTM & ADaM), and statistical reporting, ensuring compliance with FDA and PMDA. Proven ability to lead and mentor teams, optimize workflows, and collaborate with biostatisticians, data managers, and regulatory teams to deliver high-quality clinical trial reports and analyses. Strong background in process improvement, and cross-functional team coordination to drive efficiency and accuracy in clinical data programming.

• Develop analysis datasets, listings, and summary tables primarily for clinical trials.
• Ensure accuracy, consistency, and validation of all output.
• Work on complex programming assignments and provide guidance to junior team members.
• Track project progress and address validation comments.
• Attend team meetings and suggest process improvements.
• Help optimize SAS software usage within the team.
• Identify training needs and mentor junior programmers.
• Act as a technical consultant for SAS-related issues.
• Lead process improvements and implement better methodologies for programming.
• Work with management to ensure the SAS team is aligned with business goals.
• Maintain study documentation as per company policies.
• Stay updated with industry trends via literature reviews and professional networks.
  

• Develops SAS programs for analysis datasets, listings, and safety summary tables.
• Works on complex SAS programming across multiple studies and ensures validation.
• Provides project tracking updates and documents programming activities.
• Acts as a subject matter expert within the Indian SAS team.
• Mentors and trains junior programmers up to SAS Programmer II level.
• Collaborates with US/EU statistical programming teams to improve processes.

• Develops SAS programs for analysis datasets, listings, and safety summary tables.
• Works on complex SAS programming across multiple studies and ensures validation.
• Provides project tracking updates and documents programming activities.
• Acts as a subject matter expert within the Indian SAS team.
• Collaborates with US/EU statistical programming teams to improve processes.

• Develops SAS programs for analysis datasets, listings, and safety summary tables.
• Works on complex SAS programming across multiple studies and ensures validation.
• Provides project tracking updates and documents programming activities.
• Mentors and trains junior programmers up to SAS Programmer II level.
• Collaborates with US/EU statistical programming teams to improve processes.

• Supports the development of SAS programs for analysis datasets, listings, and tables.
• Assists in data validation, debugging, and documentation of programming activities.
• Works under supervision to ensure accuracy and consistency of outputs.
• Collaborates with senior programmers and global teams to gain hands-on experience.
• Learns and applies SAS best practices in clinical trial data analysis.

• Supports the development of SAS programs for analysis datasets, listings, and tables.
• Assists in data validation, debugging, and documentation of programming activities.
• Works under supervision to ensure accuracy and consistency of outputs.
• Collaborates with senior programmers and global teams to gain hands-on experience.
• Learns and applies SAS best practices in clinical trial data analysis.