Senior Contract Clinical Trial Statistician

RTI International; Few (NC); On-site; USD 125,000 - 153,000; Full time

Job summary

RTI International is seeking a Contract Senior Clinical Trial Statistician to lead end‑to‑end analysis for multiple Phase II/III trials. You will ensure data integrity and regulatory compliance, serving as the primary liaison with CROs and internal teams.

This 6‑month role may extend or convert to a permanent position. The ideal candidate has a Master’s degree in statistics or related field and at least 6 years of trial analysis experience, with strong knowledge of CDISC standards and regulatory

Qualifications

• Master's degree in Statistics, Data Science, Mathematics, or related field.
• Minimum of 6 years of progressive experience in clinical trial analysis in biotech/pharma/CRO.
• Deep understanding of ICH-GCP, FDA/EMA regulatory requirements, and CDISC SDTM/ADaM.

Responsibilities

• Act as lead trial statistician for Phase II/III trials and deliver submission-ready analyses.
• Collaborate with trial teams to design studies, perform sample size calculations, and develop analysis plans.
• Oversee development and maintenance of statistical analysis plans and datasets.
• Support regulatory submissions and health authority inspections with analytic results.

Skills

R language

SAS

Python

Leadership

Project management

Communication

Education

Master's degree in Statistics or related field

Bachelor's degree with 8 years experience

Tools

R

SAS

Python

Job description

RTI International is seeking a Contract Senior Clinical Trial Statistician to lead end‑to‑end analysis for multiple Phase II/III trials. You will ensure data integrity and regulatory compliance, serving as the primary liaison with CROs and internal teams.

This 6‑month role may extend or convert to a permanent position. The ideal candidate has a Master’s degree in statistics or related field and at least 6 years of trial analysis experience, with strong knowledge of CDISC standards and regulatory