Biostatistician

Placements24; Willows (CA); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Health, dental, vision insurance

Retirement plan

Paid time off

Job summary

Placements24 is seeking an experienced Biostatistician to join our on-site R&D team in Welkom. You will design trials, analyze data, and interpret results for collaboration with epidemiologists and clinicians.

The role requires a PhD/Masters in biostatistics and at least 4 years in pharma or academia, with strong SAS/R/SPSS skills and excellent communication for regulatory interactions.

Qualifications

• Master's or Ph.D. in Biostatistics, Statistics, or related field.
• Minimum 4 years of Biostatistics experience in pharma/biotech/academic research.
• Proficiency in SAS, R, or SPSS.
• Strong understanding of clinical trial design and statistics.
• Excellent analytical and communication skills.
• Ability to work effectively in on-site teams.

Responsibilities

• Design clinical trials and epidemiological studies; develop analysis plans.
• Perform statistical analyses using SAS, R, or SPSS.
• Interpret results and communicate to teams and regulators.
• Ensure accuracy and integrity of statistical data collection and reporting.
• Collaborate with investigators to address statistical issues.
• Contribute to study protocols, grants, and publications.

Skills

Statistical analysis

SAS

R

SPSS

Communication

Education

Master's or PhD in Biostatistics

Tools

SAS

R

SPSS

Job description

About the Role

Our client is seeking an experienced Biostatistician to join their dedicated research and development team based in Welkom . This role is essential for providing statistical expertise in the design, analysis, and interpretation of clinical trials and observational studies. You will work closely with epidemiologists, clinicians, and other scientists to ensure the rigorous statistical integrity of research projects, contributing significantly to the development of new healthcare solutions. This position offers a stable, on-site working environment within a collaborative team dedicated to advancing medical knowledge and patient care through robust data analysis.

Key Responsibilities

• Design clinical trials and epidemiological studies, developing statistical analysis plans.
• Perform statistical analyses of research data using SAS, R, or similar statistical software.
• Interpret statistical results and communicate them effectively to research teams and regulatory agencies.
• Ensure the accuracy and integrity of statistical data collection and reporting.
• Collaborate with investigators to address statistical issues throughout the research process.
• Contribute to the preparation of study protocols, grant applications, and research publications.

Requirements

• Master's or Ph.D. in Biostatistics, Statistics, or a related quantitative field.
• Minimum of 4 years of experience as a Biostatistician in pharmaceutical, biotech, or academic research.
• Proficiency in statistical software such as SAS, R, or SPSS.
• Strong understanding of clinical trial design and statistical methodologies.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work effectively within a team in an on-site setting.

Benefits

• Competitive salary and annual performance bonus.
• Comprehensive health, dental, and vision coverage.
• Retirement savings plan with employer contributions.
• Generous paid time off and sick leave policy.
• Professional development opportunities and access to training.