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Manager Biostatistics Jobs in Wisconsin (NOW HIRING)

WI · On-site

$100 - $150/hr

Strong project management skills, with the ability to manage multiple projects simultaneously ... Ph.D. in Biostatistics, or M.S. in Biostatistics. Experience Requirements: * 3+ years of relevant ...

WI · On-site

$79.64 - $125.14/hr

Professional experience (at least 5 years) in biostatistics within the biopharma R&D industry ... Ability to handle multiple projects in parallel, clearly managing timelines & expectations ...

... Biostatistics, Supply Chain Management and Facilities groups for the designated operation's team or projects. Anticipating changes driven by business growth, the Histology Manager may develop plans ...

... Biostatistics, Supply Chain Management and Facilities groups for the designated operation's team or projects. Anticipating changes driven by business growth, the Histology Manager may develop plans ...

USMLE Step 1 Tutor

Milwaukee, WI · Remote

$30 - $40/hr

... and biostatistics with emphasis on foundational science integration with clinical scenarios ... managing the enormous scope of testable content. Adapts instruction using First Aid, Pathoma, and ...

USMLE Step 1 Tutor

Madison, WI · Remote

$30 - $40/hr

... and biostatistics with emphasis on foundational science integration with clinical scenarios ... managing the enormous scope of testable content. Adapts instruction using First Aid, Pathoma, and ...

... Biostatistics, Health Policy, Statistics, Biometrics, or equivalent experience * 3+ years of research experience in managing and analyzing data, and proven expertise working with clinical and ...

$14 - $18.75/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

$14.75 - $19.50/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

$15 - $20.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

$14.75 - $19.75/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

$14.50 - $19.50/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

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Manager Biostatistics information

What is a manager biostatistics?

A Manager Biostatistics is a professional who leads a team of biostatisticians in designing, analyzing, and interpreting data from clinical trials and research studies, primarily in the pharmaceutical, biotechnology, or healthcare industries. They oversee the statistical aspects of projects, ensure compliance with regulatory guidelines, and collaborate with cross-functional teams such as clinical, regulatory, and data management. Their responsibilities also include mentoring team members, managing project timelines, and contributing to the development of statistical analysis plans and reports.

How does a manager biostatistics typically collaborate with clinical and regulatory teams during drug development projects?

As a Manager of Biostatistics, you play a pivotal role in cross-functional collaboration, especially with clinical and regulatory teams. You’ll work closely with clinical researchers to design studies, establish statistical analysis plans, and interpret results, ensuring the scientific rigor of the data. In addition, you’ll support regulatory submissions by preparing statistical reports and addressing queries from regulatory agencies. Effective communication and the ability to translate complex statistical concepts for non-statistical team members are essential for success in this role.

What are the key skills and qualifications needed to thrive as a manager biostatistics, and why are they important?

To thrive as a Manager Biostatistics, you need advanced knowledge of statistical methodologies, clinical trial design, and a graduate degree in biostatistics or a related field. Proficiency with statistical software such as SAS, R, and experience with data management systems are typically required, alongside possible certifications like SAS Certified Specialist. Strong leadership, communication, and project management skills are essential for effectively guiding teams and collaborating with cross-functional stakeholders. These competencies ensure accurate data analysis, high-quality research, and successful project delivery in regulated environments.

What are the most commonly searched types of Biostatistics jobs in Wisconsin?

The most popular types of Biostatistics jobs in Wisconsin are:

What are popular job titles related to Manager Biostatistics jobs in Wisconsin?

For Manager Biostatistics jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Manager Biostatistics jobs in Wisconsin look for?

The top searched job categories for Manager Biostatistics jobs in Wisconsin are:

What cities in Wisconsin are hiring for Manager Biostatistics jobs?

Cities in Wisconsin with the most Manager Biostatistics job openings:

Infographic showing various Manager Biostatistics job openings in Wisconsin as of August 2026, with employment types broken down into 87% Full Time, 10% Part Time, and 3% Contract. Highlights an 73% In-person, 6% Hybrid, and 21% Remote job distribution.

$100 - $150/hr

Other

Posted 7 days ago


Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Essential Functions:
  • Lead statistical activities for clinical trials and data analyses, including study design, statistical analysis plan development, and statistical analysis.
  • Provide statistical expertise to cross functional teams, including clinical operations, data management, and regulatory affairs.
  • Ensure the quality and accuracy of statistical deliverables, including statistical reports, tables, listings, and graphs.
  • Participate in the development and review of clinical study protocols and case report forms (CRFs) to ensure appropriate statistical analysis.
  • Develop and maintain SAS programs for statistical analysis in accordance with standard operating procedures (SOPs), good programming practices, and regulatory guidelines.
  • Keep up to date with regulatory guidelines and industry standards related to biostatistics and ensure compliance with these guidelines.
  • Participate in the development and maintenance of internal processes and standard operating procedures to improve statistical efficiency and consistency.
  • Provide guidance and mentorship to junior statisticians.
  • Other duties as assigned.
Necessary Skills and Abilities:
  • In-depth knowledge of statistical methodologies.
  • Excellent communication and interpersonal skills, with the ability to work collaboratively in cross functional teams and with external partners.
  • Strong project management skills, with the ability to manage multiple projects simultaneously.
  • Knowledge of regulatory requirements and guidelines related to statistical analysis and reporting of clinical trial data.
  • Ability to program in SAS and or R.
Educational Requirements:

Ph.D. in Biostatistics, or M.S. in Biostatistics.

Experience Requirements:
  • 3+ years of relevant work experience.
  • Outsourcing industry experience required.
  • Experience in clinical trial design, sample size calculations, and statistical analysis.
  • Experience with CDISC data structures, such as SDTM and ADaM.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager.

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

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