Covance Biostatistician I in Bangalore, India
Work Location: Bangalore
The statements below reflect general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the Job.
Interaction with members of assigned projects teams from other dissciplines
Preparation of statistiocal analysis plans under the supervision of senior statistical staff
Assure quality of personal work
Perform QC/Statistical review of Data Displays for study endpoints
Statistical Analysis of clinical trial data usinf basic methodology, under the supervision of senior statistical staff
Perform sample size calculations under the supervision of senior clinical staff
Generate randomization schedules from provided specifications
Maintain Project adminstration files with regard to all documents produced by Biostatistics, including associated review , QC and Project tracking information and internal and external communications
Maintain electronic files generated in Biostatistics according to defined specifications and procedures ensuring those of a temporary nature are deleted in a timely fashion.
SAS programminf and related activities for the presentation and analysis of clinical trial data
Carry out all activities according to appropriate Covance SOP's working within the framework of the Quality Management system and to GCP.
perform other duties as requested by Management
MA or MS in statistics Project preferably with a strong medical statistics component.
(Alternative academic qualifications are assessed for comparability)
0 to 3 years of postgraduate experience in the application of statistics in clinical trials
Interpersonal and effective communication skills
Cooperation and team oriented
The ability to work in tight deadlines while maintaining high standards
Job Number 2018-16938
Job Category Clinical Operations
Position Type Full-Time
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