About the Company
IQVIA (NYSE: IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human science and data science to make the greatest impact possible, for patients and for society. With a global presence and a vast network of experts, IQVIA offers unparalleled opportunities for career growth and impact. Join us in our mission to accelerate medical innovation and improve patient outcomes worldwide.
Job Description
We are seeking a highly skilled and experienced Biostatistician to join our dynamic team in Milwaukee, Wisconsin. This critical role involves applying advanced statistical methodologies to clinical trials and research studies, contributing significantly to the development and evaluation of new therapies. The successful candidate will be instrumental in designing studies, analyzing complex data, and interpreting results to inform strategic decisions. We are proud to offer visa sponsorship for exceptional international candidates who are eager to contribute their expertise to our innovative projects and a collaborative global team.
Key Responsibilities
- Collaborate with clinical development teams to design and implement robust statistical analysis plans for clinical trials.
- Perform statistical analysis of clinical trial data using SAS, R, or other relevant software.
- Develop and review statistical sections of clinical study protocols, reports, and publications.
- Provide statistical input and guidance to cross-functional teams, including medical, regulatory, and data management.
- Ensure compliance with regulatory requirements and industry best practices for statistical analysis.
- Participate in the interpretation and presentation of study results to internal and external stakeholders.
- Contribute to the development and validation of statistical methodologies and software tools.
Required Skills
- Master's degree or PhD in Biostatistics, Statistics, or a related quantitative field.
- Minimum 5 years of experience as a Biostatistician in the pharmaceutical, biotechnology, or CRO industry.
- Strong proficiency in statistical programming languages, particularly SAS and R.
- In-depth knowledge of statistical methods used in clinical trials (e.g., survival analysis, mixed models, Bayesian methods).
- Excellent understanding of regulatory guidelines (e.g., FDA, EMA, ICH) pertaining to clinical trial design and analysis.
- Demonstrated ability to communicate complex statistical concepts effectively to non-statisticians.
- Proven track record of contributing to clinical study reports and regulatory submissions.
Preferred Qualifications
- PhD in Biostatistics or Statistics.
- Experience with adaptive trial designs.
- Prior experience with CDISC standards (SDTM, ADaM).
- Familiarity with data visualization tools (e.g., Tableau, Power BI).
- Experience mentoring junior statisticians.
Perks & Benefits
- Comprehensive health, dental, and vision insurance plans.
- Generous paid time off and holidays.
- 401(k) retirement plan with company match.
- Professional development and continuing education opportunities.
- Life and disability insurance.
- Employee assistance programs.
- Opportunity to work on cutting-edge research and make a significant impact on global health.
- Relocation assistance and visa sponsorship for eligible international candidates.
How to Apply
Interested candidates are invited to submit their application by clicking the "Apply Now" button below. To ensure your application is considered, please include the following:
- A current resume
- A cover letter outlining your suitability for the role and your motivation for applying.
We review applications on a rolling basis and will contact shortlisted candidates for an interview.
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