Candidates must have minimum of 2 years of statistical programming experience in clinical/pharma domain
Strong programming and analytical skills using SAS software
Good knowledge and understanding of CDISC SDTM ADaM TLF and Define.xml standards
Proven knowledge of regulatory guidance documents such as ICH-E3 and ICH-E9
Proven understanding of clinical trials fundamentals of clinical research GCP.
Strong communication (verbal and written) & interpersonal skills
Good team player self-disciplined & self-motivated with ability to learn faster
Employement Category:
Employement Type: Full timeIndustry: Bio Technology & Life SciencesFunctional Area: PharmaceuticalRole Category: Data ManagementRole/Responsibilies: Clinical SAS Programming