Biostatistician I

• Requisition ID #:

Job Category:
Research- Employment Type: Full Time- Experience Level: Experienced (non-manager)- City, State: Milwaukee, WI- Work Location: Clinical Cancer Center- Department: Center for International Blood and Marrow Transp- Education: Masters DegreePosition Description:
Every great life-changing discovery begins the same way—with new knowledge. It can change everything, from a single life to the future of entire communities.

That's why academic medicine, and the continuous pursuit of knowledge, is at the center of everything we do at the Medical College of Wisconsin (MCW).

The Center for International Blood and Marrow Transplant Research (CIBMTR) provides a unique resource of data and statistical expertise to the scientific community for addressing important issues in hematopoietic cell transplantation and cellular therapies.

In the role of
Biostatistician I you will responsible for meticulous data management and analysis for multiple ongoing research studies, including data cleaning, description of patient populations, analysis and interpretation of data and conducting outcome analysis.

Directs the progress of research studies including management and coordination.

Support investigators, scientists and physicians in the development of moderately complex study design, preparation of scientific reports, manuscripts and materials for presentation at national and international meetings.

Responsibilities:

_Research:
_

• Serve as the primary statistician for CIBMTR research studies and independently collaborate with principal investigators in the development and implementation of complex datasets.
• Support principal investigators in moderately complex study design; prepare preliminary study tables to assess study feasibility and determining final study population.
• Prepare moderately complex datasets. Write SAS programs to create or verify key analysis data sets and TLFs.
• Performs descriptive, univariate, and multivariate (with PhD statistician supervision) analyses.
• Provide project management for studies and projects to ensure the timely and accurate completion of analyses, reports, and submission of studies for publication.
• Review clinical study reports and assist in manuscripts submitted for publication.

_ Innovation:
_

• Collaborate with Data Operations staff to resolve data inconsistencies for research studies and projects. Collaborate in standard processes to resolve data inconsistencies.

_ Registry Support:
_

• Respond to requests from physicians, patients, pharmaceutical and insurance companies, the media, state and federal government agencies through the CIBMTR Information Request Process.
• Collaborate on the development of program materials including educational materials, training manuals, marketing materials, websites, and reports.
• Participate on appropriate committees relevant to the advancement of CIBMTR Statistical Operations activities.
• Assist in the writing of grants and peerreviewed scientific publications, providing expertise and statistical content regarding the statistical analysis plan, study population, statistical methodology and description of results.
• Collaborate with the Statistical Operations administrative staff to support the management of the CIBMTR Scientific Committees.

Secondary Functions:

• Perform other duties as assigned.

Knowledge - Skills - Abilities

• Knowledge: Research study design methods, independent problem solving, decision making, statistical analyses.
• Skills: Programming experience with statistical analysis programs, logistic regression and survival analysis, research writing for publication, interpersonal communication and networking, independent research project management, written, oral and presentation skills required. Microsoft Office computer software and Internet skills.

Preferred Schedule:
Mon-Friday - Hybrid

Position Requirements:

Minimum Qualifications:

• Appropriate experience may be substituted for education on an equivalent basis._

Minimum education:
Master's degree

Minimum experience: 1 year

Preferred Qualifications:

Preferred education:

Master's degree in Biostatistics or closely related biomedical field where biostatistical design and analyses comprised the primary course of study.

Application in statistical analysis of data from large, long-term, observational epidemiological research studies.

Preferred experience:

Performing statistical design/analysis of data from large, long-term, observational epidemiological research studies, advanced knowledge of one or more programming languages.

Knowledge of data structures and data science techniques. Ability to plan, create, program, and manage complex statistical computer databases. Strong analytical communication, critical thinking, and problem-solving skills. Excellent time management skills and ability to multi-task and prioritize projects. Recent Masters level graduates will be cons

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