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Emmes Group

Associate Biostatistician

Posted 9 days ago
0-2 years experience
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The Associate Biostatistician collaborates with study teams to determine study designs, review protocols, and develop statistical analysis plans. They also generate reports for data monitoring, regulatory bodies, and scientific publications while ensuring compliance with industry standards.

Overview

Associate Biostatistician

Be Part of One Team, One Purpose.

At Emmes Group, we’re shaping the future of clinical research—where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we’ve led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.

Through our two business units—Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions —we are modernizing clinical trials and accelerating the development of life-changing therapies.

We believe that every clinical breakthrough starts with people—people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.

The Associate Biostatistician supports biostatistics activities on one or more studies. Collaborates with study team to determine study design, reviews protocols and statistical analysis plans, supports statistical analysis, and generates reports summarizing findings. Evaluates and contributes to sections of protocols that require statistical input.


Responsibilities

  • Collaborates with study team to determine study design for research projects.
  • Evaluates and contributes to sections of protocols that require statistical input.
  • Reviews protocols and case report forms to ensure protocol objectives are met and standards are maintained.
  • Generates randomization schedules for randomized clinical research studies and ensures proper implementation and documentation.
  • Supports development of statistical analysis plans, other study plans and statistical programming.
  • Generates reports to support data and safety monitoring activities
  • Generates quality control and operational reports to support clinical operations.
  • Generates study reports to be distributed to internal and external monitoring committees and regulatory bodies.
  • Contributes to manuscripts and or scientific presentations.
  • Contributes to innovation in Biostatistics that will continuously enhance current statistical knowledge and practices.
  • Acquires knowledge of current statistical and medical literature to ensure that sound methodologies are adopted.
  • Contributes to review of statistical process development, standardization and improvement across company.
  • Provides project updates to appropriate project or department management staff.
  • Keeps abreast of and ensures compliance with regulatory practices, example FDA, EMA, and ICH guidance and recommendations.
  •  
  • Performs other duties as assigned
  • Complies with all policies and standards

Qualifications

  • Master's Degree Biostatistics, statistics, epidemiology or related field. Required
  • less than 1 year Years of related experience Preferred
  • less than 1 year Demonstrated proficiency with statistical methods and applications. Preferred
  • less than 1 year Strong programming skills in SAS and/or R. Preferred
  • less than 1 year Expertise in modern techniques for data manipulation, visualization and statistical methodology. Preferred
  • less than 1 year Ability to manage multiple tasks and priorities effectively. Preferred
  • less than 1 year Ability to work independently as well as in a team environment. Preferred
  • Strong skills in prioritization, problem solving, organization, decision making, and time management. High
  • Ability to articulate statistical and technical concepts through written and oral communication. High
  • Strong communication, interpersonal and organization skills. High
  • self motivated, proactive and detail oriented. High

 

If you’re looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.


 

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


 

CONNECT WITH US!

Find us on LinkedIn:/the-emmes-group/
Visit our website:https://www.theemmesgroup.com/

 

The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.

 

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