Biostatistician — Clinical Trials (Phase I–IV) & SAS

Ocs Consulting; Netherlands; Remote; EUR 55,000 - 90,000; Full time

Job summary

Ocs Consulting is seeking a Biostatistician to provide statistical input for Phase I–IV clinical trials, perform data analyses, and contribute to reporting. You will prepare analysis plans and detailed specifications for analysis files, tables, listings and figures, interpret results, and write statistical sections of study reports.

Requirements include a Master in Biostatistics or related field and at least three years in the pharmaceutical industry, with strong SAS Base and Macro skills and

Qualifications

• Familiarity with moderately complex statistical methods for Phase I-IV trials.
• Working knowledge of SAS Base and SAS Macro.
• Experience in a regulated environment with emphasis on quality.

Responsibilities

• Provide statistical input into Phase I–IV clinical trial development.
• Perform analyses of clinical trial data and contribute to reporting.
• Prepare analysis plans and write detailed specifications for analysis files, tables, listings and figures.
• Interpret analyses and write statistical sections of study reports; deliver statistical deliverables.

Skills

Statistical methods for Phase I-IV

English proficiency (spoken & written)

Regulatory environment awareness

Independent and pro-active attitude

Education

Master in Biostatistics or related field

3 years of relevant experience in the Pharmaceutical Industry

Tools

SAS Base

SAS Macro

Job description

Ocs Consulting is seeking a Biostatistician to provide statistical input for Phase I–IV clinical trials, perform data analyses, and contribute to reporting. You will prepare analysis plans and detailed specifications for analysis files, tables, listings and figures, interpret results, and write statistical sections of study reports.

Requirements include a Master in Biostatistics or related field and at least three years in the pharmaceutical industry, with strong SAS Base and Macro skills and