Match score not available

Principal Biostatistician - Remote

Remote: 
Full Remote
Work from: 

Offer summary

Qualifications:

Masters degree in statistics or related discipline, Ph.D. desired., 8+ years supporting clinical trials in Pharmaceutical/Biotechnology industry..

Key responsabilities:

  • Provide statistical support to clinical studies. Participate in development of study protocols and CRFs. Perform statistical analyses, interpret results. Prepare clinical study reports and integrated summaries.
  • Utilize strong communication skills to present methodology and decisions.
Lifelancer logo
Lifelancer Information Technology & Services Startup https://lifelancer.com/
11 - 50 Employees
See more Lifelancer offers

Job description

Logo Jobgether

Your missions

Our Senior Biostatisticians perform ad-hoc or exploratory analyses to support submission or Health Authority Questions. Having exposure to regulatory work experience is a bonus, for example, if you understand the regulatory questions and translating them to statistical problems, collaborating effectively, with clinical and regulatory colleagues. Supporting medium complexity clinical trials (starting from Design to Archival experience) and supporting some project-level activities.
As a Principal Biostatistician, your responsibilities will include:

  • Providing statistical support to clinical studies
  • Participating in the development of study protocols, including participation in study design discussions and sample size calculations
  • Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications
  • Performing statistical analyses and interpreting statistical results
  • Preparing clinical study reports, including integrated summaries for submissions
  • Utilizing your strong communication skills to present and explain the methodology and consequences of decisions.


To be successful in this position you will have:

  • Masters degree in statistics or a related discipline. Ph.D. strongly desired.
  • 8+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
  • Experience working for a CRO is strongly desired.
  • Experience in sample size calculation, protocol concept development, protocol development, SAP, and preparing clinical study reports including integrated summaries for submissions.
  • Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers. Knowledge of R programming is a plus.
  • Solid understanding implementation of CDISC requirements for regulatory submissions.
  • Adept in ADaM specifications generation and QC of datasets
  • The ability to build strong external internal relationships and motivate a regional or global team.
  • Very effective communicator: able to explain methodology and consequences of decisions in lay terms.

Please use the below link for job application and quicker response.

https://lifelancer.com/jobs/view/54d9752cb50932511cdcf4b1c9868c9c

Required profile

Experience

Industry :
Information Technology & Services
Spoken language(s):
Check out the description to know which languages are mandatory.

Soft Skills

  • Collaboration
  • Teamwork

Biostatistician Related jobs