Clinical Sas Programmer

Job Description

Hiring for MNCClinical Sas Programmer SDTM AND ADAM AND TLF Mandatory3YrsHyderabad, Chennai, Mumbai, Pune, Gurgaonexperience in Statistical programming and/or design and analysis of Phase I to Phase IV clinical trials in a Contract Research Organization or Pharmaceutical or Biotechnology company
• Thorough knowledge of the pharmaceutical industry including understanding of clinical drug development process and associated documents and regulations.
• Good knowledge of GCP, Good Programming Practices, ICH-E3, ICH-E9 and other regulatory guidance documents (e.g., USFDA and EMEA)
• Understanding clients requirement and providing all the required statistical inputs on, SAP, Mock Shells, Tables, Listings, Figures, or any other statistical programming deliveries
• Good understanding of the statistical programming domain and related processes
• Assists with developing, monitoring, and enforcing productivity and quality standards along with related documentations.
• Coordinating with the project management in meeting the timeline and defining/capturing the metrics for monitoring and maintaining the quality and productivity
• Good verbal and written communication skills coupled with good organizational skills.
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Keyskills :
clinical sas programmingsdtmcdisc standards