Post Doctoral Medical Fellow - Applied Biostatistics, Clinical Trial Simulation

Boehringer Ingelheim; Ridgefield (CT); Remote; USD 68,000 - 92,000; Full time

Job summary

Boehringer Ingelheim is seeking a Postdoctoral Research Fellow to advance robust clinical trial simulation tools by integrating multimodal datasets. The role is applied and bridge academia to industry, emphasizing reproducible methods and practical tools for clinical development teams.

You will work with a collaborative team to evaluate rigorous methodologies, implement simulation frameworks, and translate findings into decision support for study design, site performance, and operational risk

Qualifications

• Ph.D. in Biostatistics or Statistics from an accredited institution.
• Strong foundation in clinical trial methodology and inference (GLMs, mixed models, survival analysis, longitudinal models, causal/estimand thinking).
• Experience with reproducible workflows (Git, literate reporting) and programming in R and/or Python.

Responsibilities

• Integrate multimodal data sources across trial operations and clinical outcomes to parameterize simulations.
• Evaluate and validate clinical trial simulation frameworks under operational factors.
• Build simulation models for scenario basis planning and integration via simulation.
• Create reusable simulation pipelines (R/Python) with version control and documentation.
• Communicate results to cross-functional stakeholders via manuscripts, abstracts, and presentations.
• Contribute to design and analysis plans for robust trial inference and feasibility assessment.

Skills

R programming

Python programming

GLMs

Mixed models

Survival analysis

Causal/estimand thinking

Bayesian methods

Monte Carlo simulation

Git

Reproducible workflows

Quarto/RMarkdown/Jupyter

Multimodal data

Communication with non-statisticians

Education

Ph.D. in Biostatistics or Statistics

Tools

R

Python

Git

Quarto/RMarkdown/Jupyter

Job description

The gBDS / Med Data/AI, Boehringer Ingelheim is seeking a Postdoctoral Research Fellow to help advance the development of robust clinical trial simulation tools aimed at improving the probability of success for clinical trials by integrating multimodal datasets. This is an applied research and implementation role—focused on evaluating rigorous statistical methodology from the research stage into confirmatory, pivotal clinical studies. It is an exceptional opportunity for candidates looking to bridge academia and industry from a clinical statistical research perspective, working at the intersection of methodological rigor and real-world drug development impact.

The fellow will focus on identifying, integrating, and applying fit-for-purpose methods and data to inform trial design and execution decisions—supporting faster, more reliable studies through improved feasibility assessment, operational risk forecasting, and robust inference under real-world trial constraints. This research role emphasizes reproducible methods, transparent assumptions, and publication-quality statistical work that can be translated into practical tools used by clinical development teams. The ideal candidate is self-driven and motivated—someone who works independently and takes initiative, while benefiting from scientific guidance and a collaborative team environment.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees.

Duties & Responsibilities

You will work with considerable autonomy, taking ownership of your projects with scientific guidance available from your supervisor/s and the broader team. Core responsibilities include:

• Integrate multimodal data sources across trial operations and clinical outcomes to parameterize and calibrate simulations (internal trial data + operational metrics + external benchmarks where appropriate).


• Evaluate and validate clinical trial simulation frameworks that quantify how operational and clinical factors (e.g., recruitment pace, dropout, missing data, site heterogeneity, nonadherence, endpoint variability, protocol deviations) impact probability of success.


• Build simulation models incorporating relevant data sources (clinical trial, real world evidence,) for scenario basis planning, and integration via simulation.


• Build scenario engines for trial execution planning (e.g., “what-if” analyses on site mix, monitoring intensity, recruitment strategies, data cleaning rules, visit schedules, or enrichment approaches) and translate results into actionable decision support.


• Implement and compare statistical methods relevant to trial robustness under execution realities, including (examples):
  
  
  
  • missing data mechanisms and sensitivity analyses (MAR/MNAR),
  
  
  • Bayesian models (meta analytic, hierarchical, etc.)
  
  
  • intercurrent events and estimands-aligned strategies,
  
  
  • site-level/random effects and cluster heterogeneity,
  
  
  • treatment effect attenuation due to nonadherence,
  
  
  • informative dropout and time-varying covariates.
  
  
  
  


• Conduct simulation studies to evaluate design choices (sample size, randomization schemes, interim decision rules, adaptive elements, endpoint definitions) and make predictions using performance metrics such as power, type I error, bias, estimation bias, predictive probabilities, and other operating characteristics.


• Create reusable, reproducible simulation pipelines (R/Python) for simulation, diagnostics, and reporting—version-controlled, well-tested, and well-documented for long-term sustainability.


• Communicate results clearly to cross-functional stakeholders (biostatistics, clinical operations, clinical development, data science) via manuscripts, conference abstracts, internal whitepapers, and presentations.

Qualifications

• Ph.D. in Biostatistics or Statistics (or closely related quantitative discipline) from an accredited institution, awarded prior to start date. This role is designed for recent graduates seeking an applied biostatistics postdoc focused on clinical trial simulation. Candidates with a strong academic background who are motivated to move into industry—and who want a structured yet independent environment to bridge that transition—will be a great fit.


• Strong foundation in clinical trial methodology and inference (e.g., GLMs, mixed models, survival analysis, longitudinal models, causal/estimand thinking, multiplicity basics, Bayesian experience).


• Demonstrated ability to program in R and/or Python for statistical modeling and simulation; experience with reproducible workflows (Git, unit testing, code review, literate reporting such as Quarto/RMarkdown/Jupyter) preferred.


• Familiarity with Monte Carlo simulation, power/operating characteristic evaluation, and principled model checking/validation.


• Interest or experience working with multimodal trial data including operational metrics (site performance, enrollment curves, deviations) and clinical outcomes data; experience with real-world or observational health data is a plus but not required.


• Ability to work in a highly collaborative environment and communicate statistical results to non-statistical stakeholders with clarity and pragmatism.


• Demonstrated capacity to work independently, manage your own research agenda, and roll forward on problems without waiting for constant direction—proactive initiative is a key expectation of this role.

Eligibility Requirements

• Must be legally authorized to work in the United States without restriction


• Must be willing to take a drug test and post-offer physical (if required)


• Must be 18 years of age or older

Compensation

This position offers a base salary of $80,000. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements.

Duration: Two years

Location: Remote (within US)

Our Company

Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry's top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,300 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at www.boehringer-ingelheim.com.

Why Boehringer Ingelheim?

With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.

Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.

Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.

Want to learn more? Visit https://www.boehringer-ingelheim.com