Biostatistician

Emmes Global

$90K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in biostatistics, statistics, epidemiology, or related field.
  • Proficiency with statistical methods in clinical research.
  • Strong programming skills in SAS and/or R.
  • Ability to manage multiple tasks effectively.
  • Capability to work independently and as part of a team.
  • Strong written and verbal communication skills for technical concepts.

Responsibilities

  • Collaborating with clinical investigators on study design.
  • Writing statistical sections of protocols.
  • Reviewing protocols and case report forms for compliance.
  • Generating treatment allocations for clinical studies.
  • Leading development of statistical analysis plans and programs.
  • Performing statistical analyses and validating application programs.
  • Implementing safety monitoring reports for participant safety.

Benefits

  • Flexible Approved Time Off
  • Tuition Reimbursement
  • 401k Retirement Plan
  • Work From Home Anywhere in the US
  • Maternal/Paternal Leave
  • Casual Dress Code & Work Environment
Full Job Description
Overview

Biostatistician

US Remote

Primary Purpose

Collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer-reviewed journals.

Responsibilities

  • Collaborating with clinical investigators to determine study design;
  • Writing sections of protocols that require statistical input;
  • Reviewing protocols and case report forms to ensure that protocol objectives are met and standards are maintained;
  • Generating treatment allocations in randomized clinical research studies and ensuring proper implementation;
  • Leading the project team's development of statistical analysis plans and programs to perform analyses and display study data;
  • Performing statistical analyses; writing and validating application programs;
  • Implementing data and safety monitoring reports to ensure participants' safety;
  • Developing metrics and generating quality control reports to optimize the performance of clinical sites and the coordinating center;
  • Generating study reports to be distributed to internal and external monitoring committees and regulatory bodies;
  • Participating in professional development activities both within and outside the company
  • Other duties as assigned

Qualifications

  • PhD in biostatistics, statistics, epidemiology or related field.
  • Demonstrated proficiency with statistical methods and applications in clinical research.
  • Strong programming skills in SAS and/or R.
  • Ability to manage multiple tasks.
  • Ability to work independently, as well as in a team environment.
  • Ability to effectively communicate technical concepts, both written and oral.

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

  • Flexible Approved Time Off


  • Tuition Reimbursement


  • 401k Retirement Plan
  • Work From Home Anywhere in the US


  • Maternal/Paternal Leave


  • Casual Dress Code & Work Environment


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