Senior Quantitative Medicine Researcher
1 week ago
ABOUT CRITICAL PATH INSTITUTE (C-PATH)
Critical Path Institute (C-Path) is a nonprofit organization dedicated to fostering partnerships and innovative methodologies that enhance human health by streamlining the development and approval of new therapies. For over a decade, we have collaborated with industry and academic leaders to advance technologies across the entire spectrum of medical product development, from research to regulatory endorsement. As a prominent nonprofit committed to promoting collaboration and data sharing in the precompetitive space, C-Path has spearheaded numerous initiatives aimed at expediting the delivery of new treatments to patients. Our ongoing success is sustained by a blend of public and private support from those who share our mission to accelerate the journey to a healthier world.
POSITION OVERVIEW
The Quantitative Medicine (QuantMed) Program at Critical Path Institute (C-Path) is focused on the creation and innovation of quantitative solutions tailored for medical product development and clinical requirements. We are seeking intellectually curious and innovative professionals for the role of Quantitative Medicine Scientist. The primary objective of this position is to enhance QuantMed's current capabilities in modeling and simulation to support drug development initiatives. The Quantitative Medicine Scientist will be expected to contribute to QuantMed project outcomes in pharmacometrics and statistics, particularly concerning neurodegenerative disorders such as Alzheimer's disease. This role offers the opportunity to collaborate with leading experts and key opinion leaders within C-Path's extensive scientific network.
SUPERVISORY RESPONSIBILITIES
None
CORE DUTIES and RESPONSIBILITIES
- Design and implement pharmacometric, statistical, and cutting-edge quantitative pharmacology methodologies to inform drug development for various neurodegenerative diseases.
- Guide disease progression prediction strategies, integrating mathematical functions and fundamental scientific pathophysiological principles, in collaboration with disease-expert program leads to facilitate data-driven decision-making.
- Assess and apply nonlinear mixed effects (NLME) modeling, Bayesian inference, multivariate modeling, causal inference, and other quantitative techniques as appropriate for drug development decision-making.
- Represent the QuantMed Program and provide subject matter expertise on cross-functional project teams.
- Foster and maintain collaborative working relationships with C-Path colleagues.
- Stay updated on and implement new techniques in quantitative medicine, clinical pharmacology, modeling, and simulation.
- Author, review, and approve modeling and simulation analysis plans and outputs, interpreting and presenting key findings to regulators and stakeholders as necessary.
- Draft and provide technical input for statistical and pharmacometric reports and regulatory submissions.
- Ensure compliance with agreed timelines and budgets to guarantee timely and accurate execution of deliverables.
- Develop and provide training within and outside the QuantMed Program as required.
To excel in this role, the individual must effectively perform each essential duty. The requirements listed below represent the knowledge, skills, and abilities necessary. The Quantitative Medicine Scientist must be adept at identifying multiple quantitative methods and selecting the most suitable approach based on analytical considerations, disease-specific knowledge, and available data. The individual should communicate effectively in modeling work group discussions within C-Path-coordinated public-private partnerships with external stakeholders. Strong writing skills are essential for contributing effectively to the scientific content of manuscripts, posters, grants, and other external communication documents. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
Programming Skills:
- Proficient in R and the tidyverse ecosystem.
- Experienced in running modeling and simulation applications on Linux platforms.
- Skilled in version control workflows using git.
- Familiarity with NLME tools such as NONMEM and Monolix.
- Extensive experience in nonlinear mixed effects models (NLME), longitudinal data analysis, and missing data analysis.
- In-depth knowledge of statistical modeling, particularly regression techniques, null hypothesis significance testing, trial design, power analysis, and sample size estimation.
- Demonstrated excellence in managing multiple scientific analysis deliverables and priorities through matrix management and leadership.
- Experience working with cross-functional project/program teams in life sciences is advantageous.
- Experience with large-scale multivariate models for neurodegenerative disorders such as Alzheimer's disease and/or Parkinson's disease is preferred.
- Experience contributing to statistical analysis plans and/or biomarker qualifications for clinical studies is preferred.
- Experience with Bayesian data analysis is a plus.
- Excellent oral, written, and virtual communication skills.
- Strong critical thinking and analytical skills.
- Technical problem-solving abilities.
- Sound judgment when handling critical or confidential information.
- Regularly required to sit for extended periods and occasionally stand and walk.
- Regularly uses hands to operate computer equipment and other office tools.
- Close vision required for computer usage.
- Occasionally required to stoop, kneel, and lift (up to 25 pounds).
- Travel on occasion for out-of-town meetings (~ 10%).
- Doctoral or equivalent degree in statistics or a related discipline with 1+ years of relevant statistics research or development experience, or
- MS or MA in statistics or a related discipline with 4+ years of relevant statistical research or development experience.
The above statements describe the general nature and level of work only. They are not an exhaustive list of all required responsibilities, duties, and skills. Other duties may be added, or this description amended at any time.
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