Top 2 Biostatistician Jobs in San Jose Ca

Biostatistician
CliniOps —Fremont, CA
- Windows
- Analysis skills
- Linux
Senior Biostatistician
Intuitive Surgical —Sunnyvale, CA
- $125,000 - $211,700 a year
- Day shift
- Surgery
- Doctor of Philosophy
- Travel

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Computational Scientist II
Tailored Management —South San Francisco, CA
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$47.23 - $62.94 an hour
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1d
Computational Scientist II - 30120_J
BEPC Inc —South San Francisco, CA
Ensure AI tools are production-ready, well-documented, and accessible to users with varying technical backgrounds. Maintain version-controlled evaluation logs.
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Biostatistician

CliniOps
Fremont, CA

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Job Details

Qualifications

Statistics
Data quality checks
Experimental data reports
Customer communication
Biostatistics-based research
Medical statistical report preparation
RESTful API
SAS
IT quality control
Direct client contact
Windows
Technical report writing
SAS language
Microservices
Clinical research protocol review
Analysis skills
Clinical program data analysis
Quality control operations
Leading team collaboration initiatives
Regulatory submissions
Document quality checks
Linux
Senior level
Clinical research reports
Clinical data analysis
Clinical research protocol design input
Project leadership
Ad-hoc reporting
Cross-functional team management
Leadership

Full Job Description

Fremont, CA, USA Kolkata, India

We are seeking a highly-motivated Senior Biostatistician to join our team. This position provides statistical support for all phases of clinical development. Specific responsibilities include reviewing statistical sections of protocols, writing statistical analysis plans (SAP), developing SAS programs, and interacting with clients, and participate in FDA meetings as needed.

Responsibilities & Duties

Generate randomization schedules.
Provide sample size calculations.
Provide input into development of case report forms (CRFs).
Author statistical analysis plans, including development of table and listing shells.
Write analysis plans for eCTD submissions.
Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS.
Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests.
Perform quality control for SAS programs and other study documents (e.g., presentations and reports).
Provide statistical analysis and reports to Data Monitoring Committees (DMCs).
Review output across programs to ensure consistency.
Prepare statistical sections of clinical study reports.
Interact directly with clients.

Qualifications & Skills

Technical Skills:

OS: Linux, Windows
Web: LAMP stack, microservices, REST API, etc.

Human Skills:

Leadership
Communication

Work / Experience

Experience in analysis, design, coding, and testing
Experience in leading a cross-functional team

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