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World-wide Biotech Firm Needs A Sr. Level Associate Director Of Biostatistics - Clinical Trials, PhD
Eligibility : Medical Doctor
Location : South San Francisco, CA,San Jose, CA
Designation :
Details ::
Associate Director of Biostatistics - Clinical Trials, PhD in Statistics

With offices in both South San Francisco and Los Angeles, CA, we are a major Biotech company that has experienced tremendous growth over the last 5 years. Due to more growth and expansion, we are currently recruiting for a very well educated and experienced Associate Director of Biostatistics to join our team of scientific professionals. Read the description below. If this sounds like you, apply for the chance to join a great company with great upside. Also, we are accepting resumes for Principal Biostatistician level candidates with the same background that is described below.

Purpose: Leads a biostatistics group in support of clinical development for one or more therapeutic areas.

Job Description:
- Line management responsibility for a group of Biostatisticians in one or more therapeutic areas, including setting employee goals and doing performance reviews.
- Responsible for the statistical input provided by the group to all major documents, including clinical development plans, protocols, clinical study reports, summaries of clinical safety and efficacy, and other sections of BLAs.
- Advises Biostatisticians on technical issues associated with the design, performance, and analysis of clinical trials.
- Provides review and guidance to Biostatisticians on statistical aspects of all FDA interactions, including FDA meetings, responses to FDA questions, and Advisory Committee Meetings.
- Works closely with Therapeutic Area management in defining strategic approaches to clinical trials and in meeting operational requirements of development plans.
- Works closely with Biostatistics management to ensure a coordinated approach to Biostatistics work.
- Provides leadership to therapeutic area Biometrics management team.
- Maintains comprehensive knowledge of theoretical and applied statistics and regulatory guidelines regarding clinical trial analysis and reporting. Applies new statistical procedures to our projects as appropriate.

Job Qualifications:
- Ph. D. in statistics/biostatistics with at least 8 years experience; at least 2 years experience managing project statisticians
- Comprehensive understanding of theoretical and applied statistics; extensive experience in clinical trials.
- Comprehensive understanding of regulatory guidelines in a pharmaceutical research setting.
- BLA/NDA development and submission experience required.
- Ability to effectively collaborate, communicate, and influence throughout all levels of the organization.
- Strong leadership abilities

For your hard work, you will be rewarded with an offer that will include an aggressive base salary ($125,000 - $160,000), stock options in a public company, fantastic bonuses, a comprehensive benefits package, paid time off, a great and fun working environment, and other cool perks! Interviews are occurring early next week, so apply now if you are interested. Local candidates preferred, but we will offer relocation packages for Superstars! Visa transfers are acceptable.


Salary : $100,000 - $150,000
Company URL : N/A
Last Date : 0000-00-00
Address: N/A
       
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