Description
Contract SAS ProgrammerRate: Open
Experience: 5+
Available Positions: 12
Duration: 12 month
Location(s): Durham, NC.
Job Description
- A Statistical Programmer will provide technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to analysis and reporting.
- Coordinate project start-up activities, including Unix/PMED project area set-up, creation of global programs (e.g., set-up SAS, format SAS, etc.), tracking spreadsheets, and required documentation.
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 5 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)
Please email me your updated resume Today!! Do not miss this opportunity. Positions will be filled quickly.
Forward this to your colleagues and email me ASAP.
Thanks,
Vincent