Senior biostatistician

FORTREA; Madison (WI); Remote; USD 90,000 - 120,000; Full time

Job summary

A leading company in clinical research is seeking a Senior Biostatistician for a fully remote position. The role involves leading statistical oversight for medium complexity studies, project management, and mentoring junior staff. Candidates should have extensive experience in statistical analysis and a relevant degree.

Qualifications

• At least 8 years of experience as a statistician with a Bachelor's degree.
• At least 5 years of experience with a Master's degree.

Responsibilities

• Lead Biostatistician role on medium complexity studies.
• Prepare Statistical Analysis Plans and perform complex statistical analyses.
• Mentor biostatisticians and represent the department during client audits.

Skills

SAS

Statistical Analysis

Project Management

Education

Bachelor's degree in Biostatistics

Master's degree in Biostatistics

Job description

JOB REQUIREMENTS: Fortrea Clinical Research Unit Inc. has an opening for
a Senior Biostatistician. This position is 100% remote; may work from
anywhere in the U.S. Perform Lead Biostatistician role on medium
complexity studies, providing statistical oversight and attending
relevant project meetings. Perform project management activities for
identified projects including resource planning, timelines and milestone
management. Prepare Statistical Analysis Plans (including mock TFL
shells) for medium complexity studies under the supervision of more
senior statistical staff. Perform complex statistical analyses, quality
check statistical analyses developed by other statisticians. Conduct
overall statistical review of TFLs for complex studies prior to client
delivery. Review CRF and other study specific specifications and plans.
Perform sample size calculation for simple studies under the supervision
of more senior statistical staff. Develop the statistical sections of
the protocol for simple to medium complexity studies under the
supervision of a statistical consultant. Provide statistical input and
review of the CSR for medium complexity studies. Prepare and review of
randomization specifications and generation of randomization schedules.
Mentor biostatisticians within project activities; assigned tasks
related to the development of staff within the department. Present and
share knowledge at team meetings and/or at monthly seminars. Attend bid
defense meetings for medium complexity studies in order to win new
business. Represent the department during project-driven client audits.
5% domestic travel per year required. Must possess at least a
bachelor's degree or its equivalent in Biostatistics or related field
and at least 8 years of progressive experience as a statistician or a
related role. In the alternative at least a master's degree or its
equivalent in Biostatistics or related field and at least 5 years of
experience as a statistician or related role. Must also possess the
following: Demonstrable experience in one or more statistical software
packages (SAS) used to conduct statistical analysis; Demonstrable
experience with SAS using a variety of statistical procedures e.g.,
non-parametric analysis, linear and non-linear models, categorical data
and survival analysis; Demonstrable experience of the overall clinical
trial process; Demonstrable experience preparing Statistical Analysis
Plans, analysis, reporting. * OTHER EXPERIENCE AND
QUALIFICATIONS: Must possess at least a bachelor's degree or its
equivalent in Biostatistics or related field and at least 8 years of
progressive experience as a statistician or a related role. In the
alternative at least a master's degree or its equivalent in
Biostatistics or related field and at least 5 years of experience as a
statistician or related role. Must also possess the following:
Demonstrable experience in one or more statistical software packages
(SAS) used to conduct statistical analysis; Demonstrable experience with
SAS using a variety of statistical procedures e.g., non-parametric
analysis, linear and non-linear models, categorical data and survival
analysis; Demonstrable experience of the overall clinical trial process;
Demonstrable experience preparing Statistical Analysis Plans, analysis,
reporting. * APPLICATION INSTRUCTIONS: E-Mail a Rsum:
[e-mail]