Clinical SAS programmer - New Jersey

New York  ‐ Onsite
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Keywords

Description

Urgently seeking 3 Clinical SAS Programmer for a Direct Client in Trenton, New Jersey on a contracting basis. They are one of the Largest Global CRO working with me EXCULSIVELY to expand this team Immediately. I have placed with them many times before and Interviews are happening now and I need additional statistical programmers to join the team.3 Contract Opportunities
Global CRO
12 Month Contracts
Trenton New Jersey Job Responsibilities:

- Develop and review SAS programs and output as required for the management of clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans.

- Develop SAS programs for ad hoc tables and listings. Write, modify and maintain programs that produce diagnostics and listings for data review in support of Data Management.

- Display a positive attitude at all times, promoting and contributing to a good team spirit with a productive and professional environment.

- Demonstrate good problem solving skills, a proactive approach and a willingness to take decisions, seeking advice from senior Statistical Programming staff to confirm decisions when necessary.

- Participate in the ongoing review of the processes used by the Statistical Programming group to ensure processes are continually improved.

- Participate in the Statistical Programming review of Case Report Forms (CRF's), annotated CRF's, database structures and study related documentation (e.g. data validation guidelines).

Education/Qualifications
- BSc in a computing, life science, mathematical or Statistical subject.

- Approximately 5 years experience as a Statistical Programmer, or equivalent experience.

- Experience in the development and review of SAS programs for management and reporting of clinical trial data.

- Experience in the development and review of programs to perform electronic data transfer.

- A good understanding of clinical trials processes.

- Full knowledge and understanding of the processes and procedures used within Statistical Programming.
- Good time management skills and the ability to work to tight deadlines whilst maintaining the highest standards of work.
Please email or call me for more details. APPLY TODAY OR REFER A FRIEND. There are 5 new openings at the moment and interviews are happening!
Contact details are on my Linkedin. Search for Paul Dai at Real Staffing Group.Thanks
Paul Dai

To find out more about Real please visit www.realstaffing.com
Start date
09/2013
Duration
12 months
From
Real Staffing
Published at
29.08.2013
Project ID:
590209
Contract type
Freelance
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