Senior Biostatistician – Clinical Trials Lead

Worldwide Clinical Trials Holdings, Inc.; North Carolina; Hybrid; USD 97,000 - 192,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Principal Scientist, Biostatistician to provide independent judgment and technical leadership in study design, analysis, and reporting. You will design studies, develop analysis plans, analyze PK/clinical data, interpret results, and contribute to IP.

Join a global CRO with 3,500+ experts dedicated to improving lives through quality science. The position requires strong SAS skills, GLP/FDA familiarity, and the ability to lead teams and communicate with

Qualifications

• Familiar with GLP and FDA guidance for statistical analysis and reports.
• Excellent SAS programming skills and data interpretation ability.
• Proficient with WinNonlin, nQuery, Word and Excel for analysis and reporting.
• Able to read/write complex literature and prepare study reports.
• Able to create clear graphs, tables, and charts for publications.
• Strong organizational and problem-solving skills; follow SOPs.

Responsibilities

• Design studies and develop data analysis plans.
• Perform PK, clinical, and related statistical analyses.
• Lead interdisciplinary project teams and mentor staff.
• Prepare final reports with text, tables, graphs, and outputs.
• Interact with clients and clinical personnel on study design and analyses.
• Identify issues in statistical documents and propose solutions.
• Contribute to literature and intellectual property.

Skills

SAS programming

WinNonlin

nQuery

Microsoft Word

Microsoft Excel

Statistical analysis

Data interpretation

Report writing

Education

PhD or postgraduate degree in a scientific field

Bachelor’s degree in a scientific field + 12+ years of experience

Tools

WinNonlin

nQuery

Microsoft Word

Microsoft Excel

Job description

Worldwide Clinical Trials is seeking a Principal Scientist, Biostatistician to provide independent judgment and technical leadership in study design, analysis, and reporting. You will design studies, develop analysis plans, analyze PK/clinical data, interpret results, and contribute to IP.

Join a global CRO with 3,500+ experts dedicated to improving lives through quality science. The position requires strong SAS skills, GLP/FDA familiarity, and the ability to lead teams and communicate with