Covance Biostatistician I in Bangalore, India

Job Overview

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)


Minimum Required

  • 0 to 3 years of postgraduate experience in the application of statistics in clinical trials

  • Interpersonal and effective communication skills

  • Cooperation and team oriented

  • Self Motivation

  • 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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