M.Sc. (Statistics), SAS Programming Certifications, 3 to 5 yrs of CRO / Pharma industry experience.
- Study statistician for late phase clinical trial
- Preparation and review of SAP (Statistical Analysis Plan) and study protocol inputs
- Blinded / Unblinded statistical roles for DSMB & BDRM meetings
- Statistical Data Analysis & Reporting
- Regulatory query response and interactions
CT SAS Programmer: (Sr. Technical Officer / Technical Executive) M.Sc. (Statistics) or M.Pharm. with SAS Base or Advance certifications. 3+ yrs of CRO experience.
- SAS programing for Tables, Listings & Figures
- Generating CDISC deliverables (SDTM, ADaM)
- Creating SAS Viya dashboards
- Inputs for DM & RBQM activities
- Review and Validation of SAS codes & outputs