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Statistician

Date Posted: May 29, 2026
Yearly: USD - USD
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Job Detail

  • location_on
    Location Maryland and Grand Kru, United States of America
  • desktop_windows
    Job Type: Permanent
  • schedule
    Shift:
  • analytics
    Career Level:
  • group
    Positions:
  • calendar_view_day
    Experience:
  • male
    Gender: No Preference
  • school
    Degree:
  • calendar_month
    Apply Before: Jun 29, 2026
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Job Description

Overview

The Statistician at Validation Associates LLC will work closely with clinical investigators, sponsors, and cross-functional teams to design studies and develop statistical analysis plans. This role involves performing statistical analyses, validating applications, and ensuring the safety of study participants through data management and monitoring reports.

Key responsibilities

  • Collaborate with clinical investigators and teams to determine study design
  • Develop statistical analysis plans and programs for study data
  • Review protocols and case report forms to maintain standards
  • Generate treatment allocations in randomized clinical studies
  • Perform statistical analyses and validate application programs
  • Implement data and safety monitoring reports
  • Develop metrics and generate quality control reports
  • Create study reports for monitoring committees and regulatory bodies
  • Participate in professional development activities

Required skills

  • Minimum of 3-5 years of experience in a CRO environment
  • Proficiency with statistical methods in clinical research
  • Strong programming skills in SAS and R
  • Ability to manage multiple tasks
  • Effective communication of technical concepts

What the company offers

Not specified in the original listing.

Skills Required

Company Overview

Validation Associates LLC
Maryland and Grand Kru, United States of America
0 Current Jobs Openings

Validation Associates LLC is involved in collaborating with clinical investigators and cross-functional teams to support clinical research initiatives. The company emphasizes quality control and participant safety within clinical trials. Read More

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