Description
StatisticianMedium size CRO looking for a highly motivated individual who has a strong desire to work in all phases of drug development and in multiple therapeutic areas.
Key Responsibilities:
The incumbent will participate in developing clinical study protocols, write Statistical Analysis Plans, perform statistical analyses, and generate Statistical and Clinical Study Reports. The Biostatistician will also oversee the development and implementation of data management and programming work plans, interact with internal and external clinical study management personnel to jointly achieve clinical study objectives and timelines.
Key Responsibilities:
The Senior Biostatistician will have several years of experience working as a Biostatistician developing clinical study protocols, writing Statistical Analysis Plans, performing statistical analysis, and generating Statistical and Clinical Study Reports, overseeing the development and implementation of data management and programming work plans and interacting with internal and external clinical study management personnel.
Additionally, the incumbent will resolve complex problems and provide statistical oversight to other biostatisticians; lead efforts in the development, maintenance and adherence of Corporate policies, SOPs, and therapeutic area specific guidelines; may act as a Lead/Liaison Biostatistician, interacting with clinical study clients and oversee projects in given therapeutic areas.
Qualifications and Experience:
A Ph.D. degree in statistical science or related fields plus 3 years relevant experience or a M.Sc. plus 6 years relevant experience is required for this position.
Must have strong technical competence in SAS programming and Statistical sample size calculation software. Incumbent must have strong English language skills.
To find out more about Real Staffing please visit www.realstaffing.com