About this opportunity
Kids for the Future lists this Associate Director, Modeling & Simulation opportunity in waltham, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Location Remote - Waltham, MA, United States
Base Pay $191,000.00 - $220,000.00 / Year
Employee Type FT Exempt
Required Degree Masters
Description
At Viridian, we work with a sense of urgency for patients, creating unity with our team, the industry, and the community. We are committed to using proven science and engineering to improve the lives of people living with serious and rare diseases, and we are getting closer to achieving this goal every day.
Reporting to the Executive Director, Head of Modeling and Simulation, the Associate Director will play a key role in advancing the Modeling and Simulation function within Biometric Sciences. The role is responsible for leading hands‑on modeling and simulation initiatives that support quantitative decision‑making across clinical development programs. The Associate Director will develop, apply, and continuously enhance modeling approaches, including clinical trial simulation, innovative statistical methodologies, and disease specific models, to inform study design and portfolio strategy. The position will also drive the implementation of technical capabilities, computational infrastructure, and analytical workflows that improve the efficiency, scalability, and impact of modeling and simulation activities. In partnership with Biometrics Sciences this position will also provide cross‑functional analytical support to departments such as Clinical Pharmacology and Scientific Communications.
This role may be based in our Waltham, MA headquarters, which would be a hybrid role, or it can also be fully remote. Our office‑based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
Responsibilities (including, but not limited to):
Build, manage, and analyze a scalable, well‑curated clinical‑trial data repository by integrating raw and standardized datasets (e.g., SDTM, ADaM), harmonizing metadata, and incorporating relevant external/public data sources to support advanced statistical modeling, machine‑learning analyses, and cross‑study research
Support multiple departments across the organization by delivering advanced quantitative and analytical expertise, including but not limited to: Biostatistics: Provide analytical support for evaluating and selecting optimal study designs, leveraging simulation‑based methods to maximize probability of technical and operational success
Clinical Development: AI solutions to support efficient data review from on‑going clinical programs
Clinical Pharmacology: Conduct and support analyses of pharmacokinetic (PK) and pharmacodynamic (PD) data, including model informed drug development (MIDD) approaches and exposure–response evaluations
Scientific Communications: Generate analytical inputs and data driven insights to support the publication strategy, including figures, tables, and quantitative summaries for abstracts, posters, and manuscripts
In collaboration with Head of Modeling and Simulation, contribute to the development and continuous optimization of biostatistical SOPs and templates to enhance efficiency and quality while meeting or exceeding industry best practices. Drive organizational innovation in clinical study design and analytical methodologies
Contribute to strategic external collaborations within the biostatistics community, key opinion leaders, and external biostatistical consultants to strengthen scientific rigor and support innovation across the organization
Drive a culture of innovation in study design, analytical methodologies, and operational execution to advance scientific rigor and organizational efficiency
Promote a strong “ONE Team” culture across all functions by fostering collaboration and a unified focus on delivering the best outcomes for patients
Requirements
Requires a PhD degree in statistics, biostatistics or related field with 6+ years of relevant experience or MS degree with 10+ years of relevant experience
Expertise in statistical computing languages and infrastructure (R, python, HPC, git, etc.)
Experience in clinical trial study design optimization through simulation methods to characterize study design performance
Expertise in statistical modeling related to clinical trial analysis and portfolio decision‑making including but not limited to Bayesian modeling, joint modeling, GLMs, estimands, multiple comparisons, adaptive design analysis, and benefit risk
High proficiency in the analysis of large data sets utilizing machine learning and large language models
Manage a broad set of activities with competing and aggressive timelines, prioritize activities, and work independently; Able to work in a quickly changing environment
Demonstrated problem solving skills (including taking ownership to ensure timely resolution), a strong sense of urgency, keen attention to detail, and the ability to successfully execute in a matrix environment under time and resource pressures.
Strong verbal and/or written communications skills
Strong commitment to ethical standards
Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
The salary range for this position is commensurate with experience
Viridian offers a comprehensive benefits package including:
Competitive pay and stock options for all employees
Medical, dental, and vision insurance
Short- and long‑term disability coverage
Life, Travel and AD&D
401(k) Company Match with immediate company vest
Employee Stock Purchase plan
Generous vacation plan and paid company holiday shutdowns
Various fertility, mental, financial, and proactive physical health programs
Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.
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Worksite address
waltham, MA, 02254, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.