Hi, pls find time to review and assess my resume. I am a graduate of Statistics.







--- In Statisticians_group@..., "Tracy Wolfe" <twolfe@...> wrote:
>
> Hello,
>
> My name is Tracy Wolfe, Vice-President of Zingaro & Company, an executive
search consulting firm specializing in the search and selection of executives
for the healthcare industry.
>
>
> I am currently working on an exciting assignment with my client, an
international contract research organization with offices in India and Chicago,
IL. We are looking for dynamic individuals interested in joining the
Statistics/SAS Programming team. We seek candidates with a Master's degree, PhD
preferred, and a minimum of 5 years of experience in statistics, biostatistics
or a closely related field. Additionally, we are looking for candidates with
SAS programming experience. Individuals who are creative and thrive in an
evolving environment should consider this opportunity.
>
> I would be grateful for your assistance in our efforts. Please let me know of
any outstanding candidates who may be interested in this opportunity or have
them contact me directly.
>
> Respectfully,
>
> Tracy Wolfe
> Vice President
> ____________________________________________
> Zingaro & Company
> 21936 Briarcliff Drive - Briarcliff, TX 78669-2012
> Phone (512) 327-7275 - Fax (512) 327-1774
> www.zingaro.com
> ____________________________________________
>
>
> Job Profile
> Senior Statistician
>
> The Company:
> CliniRx Research is a part of JK Organization. JK is a 125 year old, $2.5
billion enterprise with presence in over 40 countries and leadership in multiple
sectors.
>
> Over the past several years, CliniRx Research has become one of the fastest
growing CROs in the country. The group's passion for excellence and its
commitment to the cause of human advancement, create an atmosphere for
achievement in the global research business.
>
> Scope of the Job:
> This new position, located at US company headquarters in Chicago, IL reports
to the Manager of Statistics. You will serve as the lead statistician for the
analysis of clinical trials being conducted by the company. You will interact
with the data management department, the clinical development department, and
medical writing. Additionally, you will interact with the client to carry out
the clinical trial. This job requires knowledge of statistics in clinical
trials, SAS programming, good communication skills, and excellent attention to
detail.
>
> Responsibilities:
> 1. You will serve as the lead statistician on project teams for the execution
of clinical trials. This includes:
> ­ Regular contact with the client.
> ­ Coordinating the planning and execution of the statistics related tasks as
per the contract.
> ­ You will work with the project team to establish a clear project scope and
timeline.
> ­ Working with the study data manager to ensure project deliverables are
achieved and in compliance with regulatory requirements.
> ­ You will ensure high quality, on time statistical deliverables.
> ­ Managing the financial aspects for the statistical portion of the project.
> ­ Working closely with the programmers to coordinate deliverables.
>
> 2. Preparation and review of statistical analysis plans in accordance with the
study protocol for more complicated or unconventional clinical trials.
> 3. Writes and reviews statistical method section for protocols independently.
> 4. Estimates sample sizes for clinical trials.
> 5. Advises clients on statistical design issues.
> 6. Performs QC of tables, listings, graphs, and derived datasets, particularly
those of a more complicated nature or those used for efficacy analyses.
> 7. Reviews CRFs and data management plans.
> 8. Can independently develop computer programs to generate tables, listings,
and graphs using SAS as outlined by the statistical analysis plan.
> 9. Performs quality review of statistics deliverables to clients.
> 10. Works with programmers to ensure statistical analyses are accurate and
carried out correctly.
> 11. Reviews clinical study reports.
> 12. May assist in business development activities including study pricing and
new business acquisition.
> 13. Adheres to all study/project timelines.
> 14. Documents work so other statisticians and programmers can check or modify
work.
> 15. Suggests process improvements for work procedures.
> 16. Assists with the training and mentoring of new employees as needed.
> 17. Adheres to all policies, procedures, SOPs, and training plans.
> 18. Leads and/or contributes to internal process improvement initiatives.
> 19. Files study documents into Biometrics internal files.
> 20. Reviews draft protocols and CRFs for potential data collection and
representation, or database structure problems. Provides feedback to the
project team.
> 21. Other duties as assigned.
>
>
> Candidate Requirements:
> We seek a statistician with a minimum of 5 years of experience within the
pharmaceutical industry and experience programming with SAS for statistical
analysis.
>
> We seek a professional with a Master's Degree or PhD in statistics,
biostatistics, or a closely related field.
>
> Candidates should have a sound understanding of Good Statistical Practices and
various regulatory requirements (FDA, EU, ICH), knowledge of clinical trial
design, FDA regulations, and quality standards.
>
>
> Compensation:
> A compensation package will be designed to attract outstanding talent and will
include a base salary plus benefits.
>