Urgent openings For Clinical SAS Programmer with SDTM/ADAM (Telangana)

Hybrid mode of work Bangalore OR Hyderabad location Permanent basis for a top Global Pharma/healthcare organization. - Experience: 6 to 10 years years of Statistical programming (SAS Programming)experience with ADAM/SDTM is mandatory. And for Sr.Role 7 to 15 years with people management role, ability to independently lead studies, own deliverables, ensure quality/validation, and mentor junior programmers . - Must-Have Skills: Solid SAS programming, ADaM/SDTM/TLFs, and clinical trial data expertise and study lead experience. - Top Screen-Outs: Lack of clinical data standards knowledge (SDTM/ADaM), limited QC/validation experience, or inability to independently deliver study programming activities. Expectations: - Strong SAS/programming fundamentals and SQL knowledge - Understanding of clinical trial and bioinformatics datasets - Experience with data validation, TLF generation, and database handling - Good analytical and problem-solving skills - 6 to 15 years in clinical/statistical/SAS programming or bioinformatics for two roles. - CRO/pharma/clinical research experience preferred - Exposure to SAS, R, or Python is a plus Interested can share updated CV with above skill can share to . Regards, Gopala BR Human resource Hybrid mode of work Bangalore OR Hyderabad location Permanent basis for a top Global Pharma/healthcare organization. - Experience: 6 to 10 years years of Statistical programming (SAS Programming)experience with ADAM/SDTM is mandatory. And for Sr.Role 7 to 15 years with people management role, ability to independently lead studies, own deliverables, ensure quality/validation, and mentor junior programmers . - Must-Have Skills: Solid SAS programming, ADaM/SDTM/TLFs, and clinical trial data expertise and study lead experience. - Top Screen-Outs: Lack of clinical data standards knowledge (SDTM/ADaM), limited QC/validation experience, or inability to independently deliver study programming activities. Expectations: - Strong SAS/programming fundamentals and SQL knowledge - Understanding of clinical trial and bioinformatics datasets - Experience with data validation, TLF generation, and database handling - Good analytical and problem-solving skills - 6 to 15 years in clinical/statistical/SAS programming or bioinformatics for two roles. - CRO/pharma/clinical research experience preferred - Exposure to SAS, R, or Python is a plus Interested can share updated CV with above skill can share to . Regards, Gopala BR Human resource