by Epda in Biostat

In office Hyderabad mon-fri

JOB DETAILS

Job Role Insight

- Offered salary as-per industry standards

- Career level

Junior

- Qualification

Associate

- Experience 1 - 2 Years

- Quantity 2 person

- Hiring location

Hyderabad

Description

Overview

Provide data analysis with accurate statistical methods as inputs and contribute in conclusion or making predictions of BA/BE and Clinical trial studies. Provide and assist in the development of project-related statistical analysis.

Responsibilities:

- Works with medical writing team to decide on appropriate study design and statistical methodology and provide statistical inputs in the preparation of clinical trial protocols
- Estimation of sample size and power for clinical studies
- Preparation of Randomization of subjects for clinical studies as per the study protocol
- Responsible for statistical issues pertaining to the study such as outliers, missing data and data management
- Responsible for statistical integrity, adequacy & accuracy of data used
- Review of statistical analysis for clinical studies as per respective protocols
- Review of reported statistical results which include information in the form of graphs, charts and tables




- Analyze and interpret statistical data to identify significant differences in relationships among sources of information
- Responsible for review of aCRF, CDISC Datasets (SDTM and ADaM domains) and define files
- Preparation of standard operating procedures, statistical analysis plans and work instructions for statistical analysis
- Provides accurate and timely answers to routine queries from clients pertaining to statistics
- Responsible for co-ordinating with the technical team for installation or renewal or validation of softwares pertaining to pharmacokinetics and statistics on timely basis or as and when required
- Preparation and Review of Randomization schedules and statistical analysis of IVPT/IVRT studies

Education:

Master’s / bachelor’s degree computer science or statistics or related field.

Experience & Skills:

- 2-year relevant experience; or equivalent combination of education, training and experience
- Experience in SAS programming for multiple phase clinical trials in a pharmaceutical/CRO environment
- Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Proven experience with Unix, Linux and Windows operating systems
- Proficient in written and oral communication

Request to send the Resume to: [email protected]

📌 Biostatistician (BS) (Hyderabad)
🏢 ENDPOINT DATA ANALYTICS
📍 Hyderabad