Associate Biostatistician

2 days ago

Bengaluru, Karnataka, India Emmes Group Full time

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  • Bengaluru, India
  • Biometrics/Biostatistics
  • No
  • Regular Full-Time
  • 2720

Emmes Global

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Overview
Job Description

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 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 to the project requirements and with the help of senior members of the team.

Responsibilities

  • Helps senior members in the preparation of study protocols, randomization plans, generation of randomization schedule etc
  • Conducts statistical analysis as per SAP, completes programming activities, identifies issues in the clinical study and brings them to the attention of the senior members of the team. (under supervision)
  • Performs Quality Control (QC) of own work independently and Quality Control (QC) of other people's work under supervision; Executes assigned tasks with high quality, integrity
  • Provides accurate, effective and timely communication of clinical study and defects to senior members of the team.
  • Assists in the documentation of clinical study report / manuscript through statistical interpretation of study results.
  • Works effectively and collaboratively within biostatistics team

Qualifications

  • Requires a master's degree in Statistics with minimum of 0-2 years of clinical research experience.
  • Competent in SAS programming language and/or R.
  • Good understanding of basic design of experiments and classical inference methodologies
  • Expertise in statistical methods and its applications in Clinical Research
  • Expertise in GCP principles and other regulatory standards in Clinical Research OR Working knowledge of Good Practice (GxP), International Council for Harmonization (ICH) requirements, internal processes and external regulations that govern drug development
  • Good Computational Skills and Proficiency in statistical applications (SAS, R)
  • Coordinates & communicates with the internal functional project team on client deliverables

CONNECT WITH US
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Find us on LinkedIn - Emmes

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