Principal Biostatistician

Location
Basking Ridge, New Jersey, US
Posted
Nov 06, 2018
Ref
8477BR
Required Education
Doctorate/PHD/MD
Position Type
Full time
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.

Responsibilities:
This position is responsible for working with study team members to design late stage protocols, develop and write statistical analysis plans, and perform statistical analyses for interim and final reports to be submitted to regulatory agencies. The position will also support submission activities, including design, analysis and reporting of integrated summaries for safety and efficacy. Attendance and statistical contributions at study team and project team meetings are expected. Within the BDM Department, leadership skills are needed to organize and schedule deliverables among the statisticians, SAS programmers and data managers. All BDM members are expected to support department infrastructure projects on an annual basis, including SOP improvement, development of white papers for innovative statistical methodology, new software user testing and support, etc... Mentoring opportunities are also available.

Requirements:
The following educational and previous clinical trial experience are required for this position:

PhD in Statistics or Biostatistics

• 2+ years clinical trial experience in either a biotechnology or pharmaceutical company

• Hands-on Phase IIb/III clinical trial experience and proficient in SAS programming

• Excellent oral and written communication skills, and proficient in presenting power point presentations.

• Although not required, previous support of regulatory submissions in the US, Europe, or Japan.

• Although not required, previous clinical trial experience in the therapeutic areas of Oncology

This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.

To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

LMR, #LI-LR1, statistician, biostatistician, Stat programmer