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Emmes Group

CRO services and AI-driven trial infrastructure

Associate Biostatistician

Quantitative Biology & BiostatisticsUpdated on Nov 10
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • A Master's degree in Biostatistics, Statistics, Epidemiology, or a related field is required.
  • Demonstrated proficiency with statistical methods and applications is preferred.
  • Strong programming skills in SAS and/or R are preferred.
  • Expertise in modern techniques for data manipulation, visualization, and statistical methodology is preferred.
  • Ability to manage multiple tasks and priorities effectively is preferred.
  • Ability to work independently as well as in a team environment is preferred.
  • Strong skills in prioritization, problem solving, organization, decision making, and time management are required.
  • Ability to articulate statistical and technical concepts through written and oral communication is required.
  • Strong communication, interpersonal, and organization skills are required.
  • Self-motivation, proactivity, and attention to detail are required.

Responsibilities

  • Collaborate with study teams to determine study designs for research projects.
  • Evaluate and contribute to protocol sections requiring statistical input.
  • Review protocols and case report forms to ensure protocol objectives are met and standards are maintained.
  • Generate randomization schedules for randomized clinical research studies and ensure proper implementation and documentation.
  • Support development of statistical analysis plans, other study plans, and statistical programming.
  • Generate reports to support data and safety monitoring activities.
  • Generate quality control and operational reports to support clinical operations.
  • Generate study reports for internal and external monitoring committees and regulatory bodies.
  • Contribute to manuscripts and scientific presentations.
  • Contribute to innovation in Biostatistics to enhance current statistical knowledge and practices.
  • Acquire knowledge of current statistical and medical literature to ensure sound methodologies are adopted.
  • Contribute to review of statistical process development, standardization, and improvement across the company.
  • Provide project updates to appropriate project or department management staff.
  • Keep abreast of and ensure compliance with regulatory practices, including FDA, EMA, and ICH guidance and recommendations.
  • Perform other duties as assigned.
  • Comply with all policies and standards.

Desired Qualifications

  • Less than one year of related experience is preferred.

About the Company

Emmes Group

CRO services and AI-driven trial infrastructure

Emmes Group combines a contract research organization (CRO) with an AI arm to support clinical research globally. The CRO Emmes provides study design, patient recruitment, data collection, statistics, and regulatory support, while Veridix AI builds software tools to plan, manage, and analyze trials using artificial intelligence. It differentiates itself by offering both hands-on trial services and an integrated AI-powered platform, backed by a long history dating to 1977 and a global health focus. Its goal is to modernize clinical research to make trials faster, safer, and more accessible for patients around the world.

Company size
11-50
Company stage
Not listed
Total funding
Not listed
Headquarters
Rockville, MD
Founded
2024

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