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Biostatistician

0-2 years
Not Disclosed
10 May 16, 2025
Job Description
Job Type: Full Time Education: PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Biostatistician

Department: Biometrics/Biostatistics
Employment Type: Regular Full-Time
Job ID: 2312
Location: US – Remote


Company Overview:

Emmes Group is a leader in clinical research for over 47 years, partnering with the US government, public-private sectors, and commercial biopharma. The company excels in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. Emmes is dedicated to research that impacts patient lives and promotes a culture balancing performance with people-driven values.


Position Summary:

The Biostatistician collaborates with clinical investigators to determine study designs, contribute to protocol development, write statistical analysis plans, perform statistical analyses, and report findings. This role involves authoring reports and publications, ensuring quality and compliance in clinical research data and protocols.


Key Responsibilities:

  • Collaborate with clinical investigators to design studies.

  • Write protocol sections requiring statistical input.

  • Review protocols and case report forms for compliance with study objectives and standards.

  • Generate treatment allocations for randomized clinical trials and ensure proper implementation.

  • Lead development of statistical analysis plans and programming for data analysis and presentation.

  • Perform statistical analyses and write/validate application programs.

  • Implement data and safety monitoring reports to protect participant safety.

  • Develop metrics and quality control reports to enhance clinical site and coordinating center performance.

  • Generate study reports for internal/external monitoring committees and regulatory agencies.

  • Participate in professional development activities.

  • Perform other duties as assigned.


Qualifications:

  • PhD in biostatistics, statistics, epidemiology, or related field.

  • Proficiency with statistical methods and applications in clinical research.

  • Strong programming skills in SAS and/or R.

  • Ability to manage multiple tasks effectively.

  • Ability to work both independently and collaboratively in a team environment.

  • Excellent written and oral communication skills for technical concepts.


Why Work at Emmes?

  • Direct impact on public health initiatives locally and globally.

  • Flexible Approved Time Off.

  • Work from home anywhere in the US.

  • Tuition reimbursement and 401(k) retirement plan.

  • Maternal/Paternal leave.

  • Casual dress code and supportive work environment.

  • Opportunities for community engagement via the Emmes Cares program.


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