Contract Sr. Biostatistician - Top Pharmaceutical, New Jersey

Hello,

I am a specialist recruiter with Real Staffing Group. I am dedicated to finding outstanding professionals within the Biometrics space for the pharmaceutical/biotech industry and can be found at www.linkedin.com/in/pauldai . Currently we are working on the following opportunity:

Contract Sr. Biostatistician - Top Pharmaceutical, New Jersey

Would you know of anyone who might be interested?

Here's the job description:

Contract Sr. Biostatistician - Top Pharmaceutical, New Jersey
Reporting to the Director of Biostatistics and Statistical Programming , This
position researches, designs and executes statistical activities in clinical trials
from protocol conception and development to final study report as well as data
driven analyses, regulatory responses, and data mining.

The individual will be responsible for the following activities:
- Support/participate in the development of clinical program.
- Review protocols and CRFs for soundness of trial design.
- Write statistical methodology section of the protocol.
- Prepare analysis plan and programming specifications
- Perform inferential analyses; inputs to the statistical section of the clinical study report and review clinical study report
- Support/participate in project related activities including preparation of BLA submissions and oversee CRO deliverables for studies contracted out.

Qualifications
- PhD and at least 2 years of biopharmaceutical experience or a MS with at least 5 years of experience are required.
- The successful candidate will also possess strong statistical and data analysis skills
- Strong knowledge of statistical and clinical trial methodology.
- Solid hands-on experience as statistician in clinical development program.
- Good knowledge of drug development process, and experience in supporting BLA submissions.
- Strong ability in protocol development, analyses and clinical trial reports/publications of clinical trials.
- Excellent oral and written communication skills
- Knowledge of FDA/ICR guidelines; good knowledge of SAS, S-Plus (or R) computer packages.
- Good project management skills are also required.

If you know of anyone who might be interested, any suggestions are greatly appreciated. Also, all interested candidates are welcome to contact us and send their resume to me directly.

All inquiries are kept strictly confidential.

Thank you,

Paul Dai

Paul Dai
212-707-8499

Biometric and Data Management Recruitment
Pharmaceutical Division

To find out more about Real Staffing please visit www.realstaffing.com