Hybrid Biostatistician, Clinical Trials Analytics

Placements24; Kimberley; Hybrid; CAD 90,000 - 130,000; Full time

Benefits offered by this job

Competitive salary

Medical and retirement benefits

Hybrid work model

Professional growth

Collaborative environment

Supportive team culture in Kimberley

Job summary

Placements24 is seeking an analytical Biostatistician to join our client’s growing team in Kimberley, Canada. This hybrid role covers design, analysis, and interpretation of clinical trial data, with collaboration across clinical teams, data managers, and medical writers.

You will develop SAPs, generate tables, listings, and figures for study reports and regulatory submissions, and ensure compliance with regulatory guidelines.

Qualifications

• Master's or PhD in Biostatistics, Statistics, or related field.
• Minimum of 4 years of experience in Biostatistics within pharma/clinical research.
• Proficiency in SAS or R.
• Strong understanding of clinical trial design, regulatory requirements.
• Excellent analytical and problem-solving skills.
• Effective communication and collaboration with non-statisticians.

Responsibilities

• Design SAPs for clinical development teams.
• Perform statistical analyses of trial data using SAS or R.
• Develop tables, listings, and figures for reports and regulatory submissions.
• Contribute to interpretation of study results and publications.
• Ensure compliance with programming standards and regulatory guidelines.
• Review study protocols and data management plans.

Skills

Biostatistics

Statistical analysis

SAS

R

Communication

Education

Master's or PhD in Biostatistics

Tools

SAS

R

Job description

Placements24 is seeking an analytical Biostatistician to join our client’s growing team in Kimberley, Canada. This hybrid role covers design, analysis, and interpretation of clinical trial data, with collaboration across clinical teams, data managers, and medical writers.

You will develop SAPs, generate tables, listings, and figures for study reports and regulatory submissions, and ensure compliance with regulatory guidelines.