Description
Responsibilities:- Experience of creating and validating large complex integrated clinical trial data in CDISC format (SDTM / ADaM) with knowledge of clinical trial data management
- Composing & Authenticating tables, listings, graphs (TLG's) ;
- Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting.
- Communicate with an internal team to create deliverables for pharmaceutical (Pharma) and biotech clients
Requirements:
- Minimum 4 years experience in SAS Programming for Phase I-IV clinical trials in a pharmaceutical or CRO setting.
- Required Skills: SAS-Base, CDISC (SDTM / ADaM) ; also MACROS, Submission experience, Lead (leadership) Experience, and Senior Experience is a plus (and Required for some positions)
- Bachelor or Master's degree in Statistics, Bio Stats, Computer Science, Mathematics, or a related science discipline is also highly attractive. (and Required for some positions)