Sr. Biostatistician Req.
Client: Eisai, Inc.
Woodcliff Lake, NJ
F2F interview will be required after positive phone interview
Duration: 1 year
- Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review.
- Work with the clinical study team on study design, development and/or review of clinical study protocols.
- Develop and/or review statistical analysis plans, including Table/listing/figure shells, and final study report for clinical studies; perform post-hoc statistical analyses as needed.
- Work with the project statistician and clinical data managers on design/review of case report form, data transfer specification, edit check specification, and participation in user acceptance testing (UAT); generate/review data tables/listings and coordinate data review meetings during the course of the study to ensure data quality.
- Oversee CRO programming activities, perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, ensure the quality of CRO deliverables.
- May work with the Health Outcome team on the design/analysis/validation of projects.
- May work on submission teams as a statistician and/or a programmer.
- About 55% programming and 45% statistician tasks
QUALIFICATIONS NEEDED:
- Must have a MS in Biostatistics/Statistics with at least 5 years of experience or a PhD in Biostatistics/ Statistics with at least 3 years of experience in the pharmaceutical, CRO or biotech industry.
- Strong SAS programming skills.
- Oncology experience is highly preferred.
- Good technical writing skills.
- Good communication skills (verbal and written).
- Strong teamwork ability/commitment and individual initiative.
- Strong organizational skills with ability to effectively manage multiple projects.
we need is an experienced statistician who can do SAS programming at the same time can clearly interprets statistical concept and results to non-statisticians and key medical opinion leaders
Manager is fine with an OK statistician with strong programming experience if it helps.
FROM MANAGER: As mentioned in 1 (very experienced statistician have done programming have done it a long time ago, in the beginning of their career), it is the reason that I used 8 years rule; however, as long as the candidate is very hands on, I am OK with the candidate who has more than 8 years of experience and come at a higher rate. About 55% programming and 45% statistician tasks. We really need a statistician as those who are currently in our group
The manager prefers candidates with more than 7 years of programming experience. The manager is seeking a STRONG STATISTICIANS/PROGRAMMERS...the doers not management. They should have more than 7 years Programming experience . 25+ years experience will be rejected.
Regards
Mayank Sharma
Technical Recruiter
Sage Group Consulting Inc.
Direct: 732-837-2134 :: Phone: 732-767-0010 Ext: 305
Email Id: mysharma@sagetl.com Yahoo: mayank_sharma_recruiter gtalk: mayank.mayank999
Website: www.sageci.com
You received this message because you are subscribed to the Google Groups "US_Jobs&Consultants" group.
To unsubscribe from this group and stop receiving emails from it, send an email to us_jobsnconsultants+unsubscribe@googlegroups.com.
To post to this group, send email to us_jobsnconsultants@googlegroups.com.
Visit this group at http://groups.google.com/group/us_jobsnconsultants.
For more options, visit https://groups.google.com/d/optout.
No comments:
Post a Comment