Nithya P

• Developing and validating programs to clean, integrate, and manage clinical trial data.
  Ensuring data quality and integrity throughout the trial process.
• Collaborating with cross-functional teams to ensure data meets requirements of stake holders.
• Writing and optimizing SAS programs to generate summary tables and statistical reports.
  Implementing data transformations and manipulation using SAS programming language.
  Developing macros to automate repetitive tasks and ensure consistency in analyses.
• Identify and resolve programming issues, ensuring the integrity and accuracy of the clinical trial data.
• May assist IT in testing new upgrades to technologies.
• Understand and comply with core operating procedures (SOP’s) and working instructions.
• Meet objectives as assigned, and interact with the project team to organize timelines, responsibilities and deliverables.
• Develop and maintain good communications and working relationships with CDM team.
• Part of Internal QC team and done over 500 + Checks and handling of 20+ studies conducted for a drug

• Study and investigation of specification requirements document.

• Implementation of the code.

• Testing in Bench Programmer and UI in Android devices.

• Good knowledge on interlocks, function creation and testing the changes in real devices.

• Recommend methods to solve technical issues and improve quality.

• Capturing work performed for the respective task in TFS.

• Documenting all the possible test case scenario for the implemented code.

• Implementation of the XML code for finding the details of items in vending machine through cloud computing and testing it.
• Interacted with mentor by phone, email, or in-person to gather information.
• Analyzed problems and worked with teams to develop solutions.
• Produced timely reports.