Offer summary

Qualifications:

Masters or PhD in statistics or biostatistics, Familiarity with SAS and/or R, Expertise in statistical methods applicable to clinical research, Strong analytical and problem-solving skills with attention to detail..

Key responsabilities:

Assist in preparing statistical study documents under senior oversight

Conduct statistical analysis and prepare summary reports and visualizations

Perform quality control for statistical deliverables

Communicate effectively with senior team members regarding project issues.

Job description

Overview

Job Posting Title

India Remote/Ahmedabad/Bengaluru/New Delhi

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

A Biostatistician Trainee is responsible for working closely with biostatisticians and other clinical research team members on biomedical research projects across a variety of therapeutic areas. The Biostatistics trainee assists on all activities related to the design and development of study protocols, conducting statistical analysis and reporting study outcomes of clinical trials in accordance with the project requirements under the oversight of senior team members.

Responsibilities

Contributes to preparation of statistical study documents (e.g., study protocols, randomization plans) under oversight of senior team member
Performs statistical analysis and prepare summary reports and visualizations including programming
Performs Quality Control (QC) for statistical deliverables prepared by independently or by other staff
Executes assigned tasks with high quality and integrity
Provides accurate, effective and timely communication of issues to senior members of the team.
Assists in the development of clinical study report or clinical manuscript through statistical interpretation of study results.
Works effectively and collaboratively within biostatistics team

Qualifications