Ramesh Reddy

About Ramesh Reddy

Expertise as a SAS programmer in CDISC SDTM and ADaM conversions and generation of TLF\'S.• To consults with project team on Statistical Programming requirements for clinical trial projects sponsored by pharmaceutical, biotechnology or medical device companies.• Creation and Validation of Tables, Listings, Figures, ADaM, SDTM.•Strong experience in SAS/Base SAS/Macros, SAS/Access, SAS/SQL, SAS/STATS, SAS/ODS SAS/BI, Enterprises Guide• Experience in validating SAS Datasets, Tables, Listing using Proc Compare Procedure• Proficient in understanding of Study Protocols, SAP (Statistical analysis plan), and CRF’s.• Good Comprehension of FDA and CDISC guidelines, Good Clinical Practice (GCP), Good understanding of CDISC SDTM models• Highly motivated individual with excellent organizational and interpersonal skills• Good Knowledge on Clinical Trial (I - IV) Phases• SAS Programming skills DBMS with particular reference to clinical data and SAS Macros• SAS programming, validation of clinical data and reporting.

Experience

1. Senior Manager

   Sun Pharma Development Centre Of Excellence

   Apr 2025 — Present · IN

Education

• Osmania University

  Bachelor’s Degree, B Pharmacy

  2007 — 2011

• Osmania University

  Master’s Degree, Pharmaceutical Analysis and Quality Assurance

  2011 — 2013

Skills

• Ich-Gcp
• Sas Programming
• Hplc
• Edc
• Gcp
• 21 Cfr Part 11
• Microsoft Office
• Data Management
• Standard Operating Procedure (Sop)
• Validation
• Cdisc Standards
• Databases
• Good Clinical Practice (Gcp)
• Clinical Data Management
• Clinical Trials
• Sql
• Sdtm
• Sas
• CRO Management
• Sas Macro
• Electronic Data Capture (Edc)
• Cdisc
• Sas Base
• Biotechnology
• Pharmaceutical Industry
• Sop