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Job Details

Biostatistician - Lenexa KS/or remote

Company name
Research Pharmaceutical Services, Inc.

Location
Lenexa, KS

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Profile

Overview
Designs, plans, and executes biostatistical components of clinical trials. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports.
Responsibilities
Do you want to watch clinical development change, or do you want to be the one to shape it?
 
Because we\u2019re hoping you\u2019re here for the latter.
 
Who are we?
We Are PRA.
We are 15,000 employees strong, operating in more than 80 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting lifesaving drugs into the hands those who need them most.

What will you be doing?
 
\u2022 Develops statistical analysis plans and reporting specifications for clinical trials.\u2022 Analyzes and interprets results from clinical trials using sound statistical methodology.\u2022 Applies knowledge of statistical methodology to ensure proper implementation of clinical trials.\u2022 Reviews reports and underpins the results with statistical expertise.\u2022 Provides statistical oversight across the whole clinical trial.\u2022 Accountable for the quality and delivery of the table, figure, and listing (TFL) packages.

Serves as the lead biostatistician on project teams for simple to complex clinical studies.\u2022 Develops statistical analysis plans and reporting specifications for complex clinical studies.\u2022 Performs statistical analyses and interprets results from simple to complex clinical studies.\u2022 Performs senior review of TFLs.\u2022 Provides significant input in the development and review of CRFs, edit specifications and critical variable lists.\u2022 Performs lead review of TFLs and derived datasets for clinical studies.
 
\u2022 Contributes to study protocols and clinical study reports.\u2022 Reviews simple to complex randomization specifications and dummy randomization schemes.\u2022 Trains and mentors new or junior statisticians on statistical methods and PRA procedures.\u2022 Provides statistical training at monthly seminars.\u2022 Participates in bid defense meetings.
 
\u2022 Exhibits good knowledge of multiple statistical and therapeutic areas, the drug development process, SAS procedures, and good programming practices.\u2022 Demonstrates ability to plan, implement, and monitor the statistical processes for multiple clinical studies.\u2022 Displays excellent communication skills with demonstrated leadership ability.
Qualifications

Qualifications
Master\u2019s degree in statistics or biostatistics
5 years of biostatistical experience
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities

Company info

Research Pharmaceutical Services, Inc.
Website : http://www.rpsweb.com

Company Profile
In 1998, RPS began building the foundation for the PRO model in anticipation of evolving clinical strategies within Sponsor companies. By integrating our personnel and systems with those of Sponsor companies, RPS has helped industry leaders achieve significant cost savings, flexible program staffing, and standardized system operations on a global scale. By combining the largest clinical trial recruitment engines with true clinical management oversight, RPS has achieved a service level that is well above the capabilities of any CRO or staffing company in this industry. RPS has had substantial growth and comprehensive development of all the internal infrastructure and systems required to bring the PRO model to full fruition for the benefit of Sponsors.

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