Senior Biostatistician:
Jobot

920892362
Jobot
San Francisco California
Pharmaceutical
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Description
Growing pharmaceutical company seeking biostatistics expert.

This Jobot Job is hosted by: Eric Shaner
Are you a fit? Easy Apply now by clicking the "Apply on company site" button and sending us your resume.
Salary: $120,000 - $200,000

A bit about us:

Our fast-growing pharmaceutical company is hiring for BOTH a Senior and Manager level Biostatistician!
Location - San Francisco, CA

Our success over the last 15+ years and consistent growth have enabled our staff to experience accelerated career paths. You will gain both advanced level experience, but also autonomy to own your own projects and make an immense impact within the company and on humankind. The pharmaceutical solutions, primarily oriented in the oncology sector, we create are changing the lives of people globally.

For you, medical benefits paid 100% for individual and family. This is a full time direct hire position. The Biostatistician duties will include writing statistical analysis plans and statistical sections of protocols, and developing SAS programs for inferential analysis.

Why join us?

We consistently achieve national accolades for our products. Our unique environment allows professionals to be exposed to numerous areas of the business. With our technology, our vision, and especially our talented professionals, we ensure our success in the market and attribute our growth to our unique approach.

If you are looking for PHASE III exposure and owning your own projects, then we would welcome the opportunity to speak with you.

Job Details

JOB REQUIREMENTS

Write Statistical Analysis Plans and develop table and listing shells
Provide sample size calculations
Quality control of randomization schedules
Provide input into the development of case report forms (CRFs)
Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials
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
Provide statistical analysis and reports to Data Monitoring Committees (DMCs)
Review outputs across programs to ensure consistency
Prepare statistical sections of clinical study reports
Complies with company SOPs and regulatory guidance

EDUCATION AND EXPERIENCE REQUIREMENTS:

PhD. in statistics or biostatistics with at least 3 years or MS in statistics or biostatistics with at least 5 years experience in the pharmaceutical industry
Knowledge of industry standards, such as the ICH guidelines, 21 CFR Part 11, CDISC data structures, and FDA guidelines

**TO GET YOUR APPLICATION LOOKED AT QUICKLY, PLEASE EMAIL RESPONSES TO THESE QUESTIONS TO AFTER YOU HAVE APPLIED!**

1. Please tell me about your current job responsibilities and how they relate to this role.
2. What is your highest education/degree level?
3. What is your preferred location?
4. What types of products have you supported?
5. What is your expected salary?

Interested in hearing more? Easy Apply now by clicking the "Apply on company site" button.
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