Clinical Biostatistician, Early Phase

Bayside Solutions; California; Remote; USD 150,000 - 210,000; Full time

Job summary

Bayside Solutions, Inc. is seeking a lead or supporting statistician to guide early-phase oncology studies and coordinate activities with cross-functional teams to ensure timely deliverables.

The candidate should hold a Ph.D. or M.S. in statistics/biostatistics with major biotech/pharma industry experience (5–8+ years). Proficiency in SAS and/or R is required for design, analysis, and reporting tasks.

Qualifications

• Excellent written and verbal communication skills are required.
• Ability to work independently and within a team.
• Strong interpersonal and project management skills are essential.

Responsibilities

• Provide statistical expertise for design, analysis, and reporting of clinical studies.
• Develop statistical analysis plans and analysis specifications.
• QC statistical analyses and perform statistical modeling as needed.
• Collaborate with statistical programming to ensure analyses follow the plan and specifications.
• Collaborate with data management and clinical operations for robust CRF and data collection.
• Contribute to publications and regulatory documents ensuring data presentation accuracy.
• Represent biostatistics on study teams.

Skills

Verbal and written communication

Interpersonal skills

Project management

Independent work

Education

Ph.D. or M.S. in statistics/biostatistics

Tools

SAS

R

Job description

Location: Redwood City, CA - Remote Role

Job Summary:

This position is to serve as a lead or supporting statistician for early-phase oncology studies and to coordinate activities with other functional groups to ensure timely deliverables.

Duties and Responsibilities:

• Provide statistical expertise for the design, analysis, and reporting of clinical studies.
• Develop statistical analysis plans and analysis specifications.
• Conduct and/or perform QC on statistical analyses, including statistical modeling, as needed.
• Collaborate with the statistical programmer team to ensure that analysis is conducted per statistical plan and specifications.
• Collaborate with data management and clinical operations to ensure robust CRF and database development and quality data collection.
• Contribute to the development and review of publications and regulatory documents, and ensure consistency and accuracy in data presentation.
• Represent biostatistics on study teams.

Requirements and Qualifications:

• Ph.D. or M.S. in statistics or biostatistics, a minimum of 5 years (for Ph.D.) and 8 years (for M.S.) of experience in the biotech/pharmaceutical industry as a statistician.
• Solid tumor drug development experience is required.
• Experience with early development clinical studies is desirable.
• Ability to work independently and within a team.
• Excellent verbal and written communication skills are required.
• Good interpersonal and project management skills are essential.
• Proficiency in SAS and/or R.

Desired Skills and Experience

Biostatistics, Early-Phase Oncology Trials, Solid Tumor Drug Development, Clinical Study Design and Reporting, Statistical Analysis and Modeling, Statistical Analysis Plans and Specifications, Statistical Quality Control, SAS, R, CRF and Clinical Database Development, Data Quality, Statistical Programming Collaboration, Clinical Data Management, Clinical Operations, Publications and Regulatory Documentation, Data Presentation, Cross-Functional Collaboration, Project Management, Independent Work, Written and Verbal Communication, Interpersonal Skills

Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.

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