Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s motto is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
Post : Lead Statistical Programmar
Department : Biometrics LP
Qualification : M.Sc,B.Pharma,M. Pharma,Others
Experience : Min: 8 Year(s) - Max: 10 Year(s)
Primary Skills : Ability to Handle
Clinical Research
Accepts Responsibility
Accountability
SAS Language
Location : Sigma
Brief JD : Brief JD for Group Leader (Biostatistics & Programming) Should have hands on experience with TLF and CDISC for late phase studies. Validate and review CDISC data sets as well as TFLs. Should be aware of the CDISC documentation process. Should be able to manage a team of 30-35 people for Biostats and programming. Good communication with internal and external stakeholders including clients. Review of SOPs Should be well versed in regulatory guidelines. Oversee project management tasks and study deliverables on pre specified timelines.
Last Date : 25th October, 2023
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