Biostatistician - Clinical Trials

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

About the Role

Our client is seeking an analytical and skilled Biostatistician to join their growing team in Kimberley . This hybrid role is essential for the design, analysis, and interpretation of clinical trial data, ensuring the integrity and validity of study results. You will work collaboratively with clinical teams, data managers, and medical writers to develop statistical analysis plans and generate high-quality statistical reports. This position offers a blend of remote flexibility and on-site team interaction, ideal for a statistician who thrives on data-driven insights and contributing to crucial pharmaceutical research.

Key Responsibilities

• Design clinical trial statistical analysis plans (SAPs) in collaboration with clinical development teams.
• Perform statistical analyses of clinical trial data using SAS or R, ensuring accuracy and efficiency.
• Develop statistical tables, listings, and figures for clinical study reports and regulatory submissions.
• Contribute to the interpretation of study results and provide statistical input for scientific publications.
• Ensure compliance with statistical programming standards and regulatory guidelines.
• Review and provide statistical input on study protocols and data management plans.

Requirements

• Master's or PhD degree in Biostatistics, Statistics, or a related quantitative field.
• Minimum of 4 years of experience in Biostatistics , specifically within the pharmaceutical or clinical research industry.
• Proficiency in statistical software such as SAS or R.
• Strong understanding of clinical trial design, statistical methodologies, and regulatory requirements.
• Excellent analytical and problem-solving skills.
• Effective communication and collaboration skills, with the ability to explain complex statistical concepts to non-statisticians.

Benefits

• Competitive annual salary and performance bonus opportunities.
• Comprehensive medical and retirement benefits package.
• Hybrid work model providing work-life balance.
• Opportunities for professional growth and continuous learning.
• Collaborative and intellectually stimulating work environment.
• Supportive team culture in Kimberley .