Description
New Contract Opportunity!!Clinical SAS Programmers
Mid-Size CRO
New Jersey
12 month contract
Responsibilities:
- Interact with biostatisticians, pharmacokineticists, medical writers, clinical systems developers, and other operations staff - Produce figures and documentation of datasets, including define.xml files to support the tabulation and analysis of clinical trials. - Liaise with external data vendors (e.g. central laboratories, ECG vendors) to ensure that data is transmitted in required format. - Apply knowledge of the CDISC Standards, SDTM and ADaM.- Create derived datasets in accordance with derived dataset specifications.
- Serving as primary functional representative, providing input for clinical programming projects;- Serving as a resource for, and interacting with, other functional areas to facilitate project timelines;- Integrated database design, documentation and implementation;- Create specification documents for handling and programming the clinical data, including:- Data conversion specifications;- Derived dataset specifications. Qualifications - An undergraduate degree in a quantitative or scientific field, or its international equivalent from an accredited institution.- Experience with the SAS programming language or other software languages/ tools as required.- 2+ years of SAS programming experience within the clinical trials or pharmaceutical industry.- Proven history of successful interaction with internal clients and related departments/functions in a detail oriented career or academic setting.- Knowledge of data structure standards (SDTM, ADaM).
APPLY TODAY, referrals are welcome. High visibility position. Don't miss this opportunity. Send me your resume ASAP.
Call or email me for more details. Check out my Linkedin Profile, search for Paul Dai.
Thanks
Paul
To find out more about Real please visit www.realstaffing.com