IQVIA · 7 hours ago
Principal Biostatistician FSP, RWE
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Responsibilities
Collaborate with multi-disciplinary project teams to establish project goals and timelines.
Serves as statistical lead and represents Biometrics on health outcomes and epidemiology studies.
Serves as subject matter expert for RWE/HEOR research design, methodologies, data sources, analytic techniques, and reporting.
Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.
Provides strategic and tactical support for cross-functional RWE development for regulators, payers, and clinicians.
Leverages administrative claims, electronic medical records, or other real-world data and recommends optimal study designs.
Selects and implements appropriate analytical methods including statistical models or machine learning models to align with overall business objectives.
Develops high quality study protocols, statistical analysis plans, study reports, and other study documents.
Ensures quality and consistency of analytics deliverables.
Identifies innovation opportunities for the use of RWD.
Establishes effective communication with various internal stakeholders to understand and support the strategy for when and how to use RWE.
Collaborates with and manages vendors to ensure project timelines and goals are met.
Participates in other activities and meetings to support Biostatistics and the Development Team as needed.
Qualification
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Required
PhD in Statistics, Biostatistics, or related field with 5+ years industry experience.
MS in Statistics, Biostatistics, or related field with 7+ years of industry experience.
Experience with different applications of RWE, including in support of early-stage clinical development, regulatory approvals, and payer/HTA/provider engagements.
Knowledge of global regulatory and HTA requirements for RWE
Demonstrated ability in evaluation and development of RWE from conceptualization through application.
Experience leading the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.
Extensive working experience with stakeholders such as medical affairs and health economics
Hands-on experience with prospective and retrospective observational studies
Experience leading secondary data analysis, including medical claims, electronic medical records, chart reviews, and registries.
Excellent organizational skills and proven ability to effectively lead multiple projects to successful completion.
High level of competency using standard statistical software such as SAS or R
Ability to effectively interpret and communicate research results to internal and external audiences.
Understanding of ICH GCP and E9 as well as general knowledge of industry practices and standard
Benefits
Home-based remote working opportunities
Work/life balance as well as flexible schedules.
Collaborating with motivated, high-performance, statistical and research teams
Technical training and tailored development curriculum
Research opportunities that match your unique skillset
Promising career trajectory
Job stability: long-term engagements and re-deployment opportunities
Focus on bringing new therapies to market rather than project budgets and change orders.
Experience with regulatory submissions.
Engaging, fast-paced environment.
Good work-life balance.
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
H1B Sponsorship
IQVIA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (218)
2022 (199)
2021 (286)
2020 (197)
Funding
Current Stage
Public CompanyTotal Funding
$1.5B2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
2019-08-08Post Ipo Equity· undefined
Leadership Team
Recent News
2024-10-31
The Pharma Letter
2024-05-29
2024-05-05
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