Principal Statistician Staff Scientist Biostatistics Projects
Cambridge, Massachusetts, United States
Full-time
Salary: Not Available
- Posted on:
- Expires on:
JOB TITLE:
Principal Statistician Staff Scientist Biostatistics Projects
JOB Type:
Full Time
JOB SKILLS:
Not Provided
JOB Location:
Cambridge, Massachusetts, United States
JOB DESCRIPTION
Role: Sr Biostatistician
Position Type: Contract 1 year with possibility of extension
Location: Cambridge, MA, United States
Bill Rate: $50-55 Per Hour on W2
Client Note: This role is now accepting candidates on the East Coast that are willing to travel into Boston a few times a year. Candidates within the Boston area will be given preference, if the right resource does come through.
Job Description: Principal Statistician - Staff Scientist, Biostatistics Projects
- Statistical leader in the cross-functional development team of one compound/indication.
- Statistical expertise in the development strategy, decision making and interpretation of the data generated through the clinical development program, embracing excellence and innovation among quantitative methods.
- Closely collaborate with program partners and stakeholders to deliver on-time the statistical deliverables for all clinical trials and/or HA submissions of one compound/indication
- Report to a disease area team leader, within the Biostatistics and Statistical Modelling organization.
- Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements.
Desired Skills, Qualifications and Experience:
- Master or doctorate (Ph.D.) degree in Statistics or related field with a minimum of 6 years of experience (which may include doctoral research in field of biostatistics).
- Expertise in drug development in a regulatory environment, with a demonstrated track record of advanced knowledge of biostatistics and strong command of its application to clinical trials.
- Experience in clinical trial design and scenario-planning.
- Extensive experience in the Pharma or Biotech environment.
- Demonstrates ability to plan, supervise, implement and monitor the statistical processes for multiple clinical trials.
- Expertise in Bayesian statistics.
- Proficient in statistical software (SAS and/or R).
- Able to collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials.
- Clearly explain complex statistical concepts in written and spoken English and not be afraid to contribute and speak up when necessary.
- Team-player with a focused attitude.
- Able to work autonomously as part of a cross-disciplinary team in a dynamic surrounding of a fast growing biotech company with challenging timelines.
Position Details
Posted:
Employment:
CTC
INDUSTRY:
-
Salary:
USD 55 per hour
REFERENCE NUMBER:
SNPR-479774
CITY:
Cambridge
JOB ORIGIN:
SNPR