Biostatistician (SAS) - Pharmaceutical -- 3-5 years expPosted: November 8, 2009
*** Please contact Jason Martin (Recruiter) directly about this opportunity, the full job description is below ***
Jason R. Martin
Professional Recruiter
Apex Systems, Inc.
jmartin@apexsystemsinc.com
http://www.apexsystemsinc.com
http://www.linkedin.com/in/jasonrmartin
http://twitter.com/jasonrmartin
We have several job opportunities we currently have open with Johnson & Johnson for a Biostatistician. They are looking for 3-5 years of clinical research experience along with strong experience in SAS programming and data analysis. The complete job description is attached for the details. There are 5 openings for this position in two sites in New Jersey (Raritan, NJ 08869 and Titusville, NJ 08560). This position is a W2 contract opportunity (with health benefits through Apex) for 7 months +. Openings have different focus with Psychiatry, Cardiology, Neurology, Metabolism/Diabetes. Pharmaceutical or CRO experience is highly preferred. If you are interested and qualified, please contact Jason Martin directly with your updated resume in Microsoft Word format. These roles must be able to be a W2 contract, a corp-to-corp contract will not work. Please forward this email on to your network and friends who might also be interested and have them contact me directly and let me know who referred them.
Job Description:
Location/Duration: 7 month+ W2 contract with health benefits
5 openings in 2 locations
Titusville, NJ 08560 Psychiatry (2 openings)
Raritan, NJ 08869 Cardiology (1 opening), Neurology (1 opening), Metabolism (Diabetes, 1 opening)
Interview Schedule: Phone screen, then personal interview with hiring manager and technical team leaders.
Different therapeutic areas are needed.
There are two openings are based in Titusville and three are in Raritan, but they would like candidates to be available to travel to other J&J sites when needed (not often), and within the Titusville sites.
Conducts statistical analysis of clinical trial data for reports and submissions to World-Wide Health Authorities. Uses SAS programming to produce tables, listings and graphs for use in clinical study reports. Interacts with statistical, programming and clinical team members to achieve product team goals.
While the position will involve some review of protocols and strategy of the statistical plan, it will mostly be focused on carrying out analysis, validation & creating summary reports (of the activity of the SAS programmers).
Other skills needed: data analysis, able to work independently on complex statistical problems, SAS skills, good communication (verbal and written - English fluency is a MUST)
The position requires 3-5 yrs of clinical research experience and the incumbents will get direction from the statistical leader, and will work in partnership with programmers.
Education - MUST have at least an MS in Statistics/Biostatistics; PhD is highly preferred. No BA/BS will be considered. PhDs only need 3 yrs of clinical research experience; MS must have 5 yrs of clinical research experience.
Large pharma experience is preferable to CRO experience.
Pay it forward, and forward this on!
If you have received this job description and are not interested, please forward the description and my contact information onto your network of contacts and friends. A lot of candidates learn of new job opportunities from word-of-mouth, and any referrals would be greatly appreciated. Our job opportunities are usually time sensitive, so please contact me immediately if interested. Thank you.
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