Principal Biostatistician
- Milestone Innovations Inc
- King of Prussia, Pennsylvania
- Full Time
Principal Biostatistician
KING OF PRUSSIA, PA
1 DAYS AGO
22530711
Summary
KING OF PRUSSIA, PA
In-Person
$64.90 per Year
1 Years Experience
Any degree above a Master's - e.g. Ph.D., Ed.D., J.D.
No Commission
40.00 hours per week / Day Shift / Full-Time
Description
Principal Biostatistician (2 Openings) in King of Prussia, PA: Lead and develop statistical analysis plans, study protocols, and reporting activities for clinical trials projects. Lead and mentor junior biostatisticians, ensuring high-quality design, analysis, interpretation, and reporting of clinical trial data, oversee project level statistical activities, including vendor oversight and compliance with statistical standards. Collaborate cross-functionally (e.g., data management, SAS programming, medical writing) to ensure timely, high-quality statistical deliverables and support regulatory submissions and publications.
Req.: PhD or equiv. in Statistics, Biostatistics, or related field. At least 1 year of experience in leading Phase II -III studies and development of clinical study protocols and SAPs. Proficiency in SAS or R programming, statistical modeling and statistical methods, CDISC and related FDA standards for the specifications, and creation of SDTM and ADaM datasets for clinical trials.
Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406
JOB POSTING DATES: 04/29/2026 - 05/31/2026
Additional Details
How To Identify Potential Job Scams
KING OF PRUSSIA, PA
1 DAYS AGO
22530711
Summary
KING OF PRUSSIA, PA
In-Person
$64.90 per Year
1 Years Experience
Any degree above a Master's - e.g. Ph.D., Ed.D., J.D.
No Commission
40.00 hours per week / Day Shift / Full-Time
Description
Principal Biostatistician (2 Openings) in King of Prussia, PA: Lead and develop statistical analysis plans, study protocols, and reporting activities for clinical trials projects. Lead and mentor junior biostatisticians, ensuring high-quality design, analysis, interpretation, and reporting of clinical trial data, oversee project level statistical activities, including vendor oversight and compliance with statistical standards. Collaborate cross-functionally (e.g., data management, SAS programming, medical writing) to ensure timely, high-quality statistical deliverables and support regulatory submissions and publications.
Req.: PhD or equiv. in Statistics, Biostatistics, or related field. At least 1 year of experience in leading Phase II -III studies and development of clinical study protocols and SAPs. Proficiency in SAS or R programming, statistical modeling and statistical methods, CDISC and related FDA standards for the specifications, and creation of SDTM and ADaM datasets for clinical trials.
Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406
JOB POSTING DATES: 04/29/2026 - 05/31/2026
Additional Details
How To Identify Potential Job Scams
Job ID: 519756310
Originally Posted on: 5/3/2026
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