Clinical Biostatistician

Bayside Solutions; California (MO); On-site; USD 90,000 - 120,000; Full time

Job summary

A biotechnology firm is looking for a Statistician to support early-phase oncology studies. This position requires a Ph.D. or M.S. in statistics or biostatistics, coupled with at least 5-8 years of industry experience. The role involves providing statistical expertise, developing analysis plans, and collaborating across teams to ensure quality deliverables. Proficiency in SAS and R is essential. Strong communication and project management skills are also important. This position is onsite in Redwood City, CA.

Qualifications

• Ph.D. or M.S. in statistics or biostatistics.
• Minimum of 5 years experience for Ph.D. and 8 years for M.S. in the industry.
• Solid tumor drug development experience is required.

Responsibilities

• Provide statistical expertise for clinical studies.
• Develop statistical analysis plans.
• Collaborate with teams to ensure quality data collection.

Skills

Biostatistics

Statistical analysis

SAS

R programming

Project management

Communication skills

Team collaboration

Education

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

Tools

SAS

R

Job description

Location

Redwood City, CA - Onsite 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, Clinical trial design, Early-phase oncology studies, Statistical analysis, Statistical modeling, Statistical analysis plans (SAP), Analysis specifications, Quality control (QC) of analyses, SAS, R programming, Data analysis, Clinical data interpretation, Cross-functional collaboration, Statistical programming collaboration, Data management collaboration, Clinical operations coordination, CRF design, Database development, Data quality assurance, Regulatory document support, Scientific publications, Data presentation, Study team leadership, Oncology drug development, Solid tumor research, Clinical development, Project management, Communication skills, Technical writing, Independent work, Team collaboration

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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