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Principal-Biostatistician

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Principal Biostatistician

Details

Country: USA
Location: Cambridge MA
Total applied: 33
Location: US-MA-Cambridge
Base Pay:
$100,000 - $120,000/Year
Other Compensation
Employee Type:Full-Time Employee
Industry:Biotechnology Pharmaceutical Computer Software
Manages Others: YesJob Type:Biotech Pharmaceutical Science
Req'd Education:4 Year Degree
Req'd Experience:More than 5 Years
Req'd Travel:Not Specified
Relocation Covered:No
Contact Name:Not Available
Contact Phone:Not Available
Reference ID:
PRI042
Principal BiostatisticianThe selected candidate will be responsible for providing expert technical guidance to Biostatisticians and other staff on project teams. The Principal Biostatistician will oversee the entire design, development, and evaluation process for the technical/statistical infrastructure for the conduct and evaluation of clinical trials or for the analysis of complex research studies for which novel approaches are required, from inception to completion and are recognized as one of the organizations elite technical professionals.Qualified candidates will have a M.S. or Ph.D. in Biostatistics, Mathematical Statistics, or Statistics and a minimum of 6 years of experience within the Biopharmaceutical industry, including all phases (I-III) of clinical development. Solid experience in regulatory submissions is required, along with strong computer and SAS programming skills
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The selected candidate will be responsible for providing expert technical guidance to Biostatisticians and other staff on project teams. The Principal Biostatistician will oversee the entire design, development, and evaluation process for the technical/statistical infrastructure for the conduct and evaluation of clinical trials or for the analysis of complex research studies for which novel approaches are required, from inception to completion and are recognized as one of the organizations elite technical professionals.

Qualified candidates will have a M.S. or Ph.D. in Biostatistics, Mathematical Statistics, or Statistics and a minimum of 6 years of experience within the Biopharmaceutical industry, including all phases (I-III) of clinical development. Solid experience in regulatory submissions is required, along with strong computer and SAS programming skills

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