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:
Robust SAS/programming fundamentals and SQL knowledge
Understanding of clinical trial and bioinformatics datasets
Experience with data validation, TLF generation, and database handling
Positive 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

Regards,

Gopala BR

Human resource

📌 Urgent Openings For Clinical Sas Programmer With Sdtm/adam Hyderabad
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📍 Hyderabad