The Head of Methods & AI Integration is a senior leadership role within R&D Data and Quantitative ... Positioning DQS as a global leader in AI-enabled clinical development and decision science through ...
The Head of Methods & AI Integration is a senior leadership role within R&D Data and Quantitative ... Positioning DQS as a global leader in AI-enabled clinical development and decision science through ...
Head of US Field Medical
Waltham, MA · On-site
Partner closely with Clinical Development and Clinical Operations to support appropriate scientific ... Ensure that all MSL activities remain scientific, balanced, non-promotional, appropriately ...
Head of US Field Medical
Waltham, MA · On-site
Partner closely with Clinical Development and Clinical Operations to support appropriate scientific ... Ensure that all MSL activities remain scientific, balanced, non-promotional, appropriately ...
The Head of Quality will work cross-functionally with Regulatory, Clinical Operations, Clinical Development, Pharmacovigilance, and Technical Operations as well as external CROs, clinical sites, CMO ...
The Head of Quality will work cross-functionally with Regulatory, Clinical Operations, Clinical Development, Pharmacovigilance, and Technical Operations as well as external CROs, clinical sites, CMO ...
Authors clinical and nonclinical PK sections for regulatory submissions and clinical investigator brochures * Oversees the development of detailed work plans and study designs to incorporate ...
Authors clinical and nonclinical PK sections for regulatory submissions and clinical investigator brochures * Oversees the development of detailed work plans and study designs to incorporate ...
Non Clinical - Patient Services Representative
Hilton Head Island, SC · On-site
$16.50 - $21/hr
Details Client Name Hilton Head Regional Medical Center Job Type Travel Offering Non-Clinical Profession Non Clinical Specialty Patient Services Representative Job ID 35894373 Shift Details Shift 8 ...
Non Clinical - Patient Services Representative
Hilton Head Island, SC · On-site
$16.50 - $21/hr
Details Client Name Hilton Head Regional Medical Center Job Type Travel Offering Non-Clinical Profession Non Clinical Specialty Patient Services Representative Job ID 35894373 Shift Details Shift 8 ...
The Head of Clinical Development leads the development, execution, and communication of the global medical and scientific evidence generation strategy for our products. They solicit and incorporate ...
The Head of Clinical Development leads the development, execution, and communication of the global medical and scientific evidence generation strategy for our products. They solicit and incorporate ...
Senior Advisor, Drug Product - CMC
Boston, MA · On-site
$140K - $195K/yr
Design and oversee execution of nonclinical formulation stability and compatibility studies. * Support clinical formulation development of oral solid dosage forms, as needed. * Author and/or review ...
Senior Advisor, Drug Product - CMC
Boston, MA · On-site
$140K - $195K/yr
Design and oversee execution of nonclinical formulation stability and compatibility studies. * Support clinical formulation development of oral solid dosage forms, as needed. * Author and/or review ...
$125K/yr
An initial Non-Tenure-Track (NTT) contract is typically for two years and may lead to a five-year ... Some experience with collection development and/or technical library services. * Experience with ...
$125K/yr
An initial Non-Tenure-Track (NTT) contract is typically for two years and may lead to a five-year ... Some experience with collection development and/or technical library services. * Experience with ...
Head of Reference
Los Angeles, CA · On-site
$125K/yr
An initial Non-Tenure-Track (NTT) contract is typically for two years and may lead to a five-year ... Some experience with collection development and/or technical library services. * Experience with ...
Head of Reference
Los Angeles, CA · On-site
$125K/yr
An initial Non-Tenure-Track (NTT) contract is typically for two years and may lead to a five-year ... Some experience with collection development and/or technical library services. * Experience with ...
This executive is responsible for developing and overseeing execution of integrated quantitative strategies that support efficient translation from non-clinical development, clinical development ...
This executive is responsible for developing and overseeing execution of integrated quantitative strategies that support efficient translation from non-clinical development, clinical development ...
Partner with clinical development to translate scientific hypotheses into actionable clinical ... Equal Opportunities Moderna is committed to equal employment opportunity and non-discrimination for ...
Partner with clinical development to translate scientific hypotheses into actionable clinical ... Equal Opportunities Moderna is committed to equal employment opportunity and non-discrimination for ...
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Nonclinical Safety ...
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Nonclinical Safety ...
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Nonclinical Safety ...
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Nonclinical Safety ...
Contributes to the development and execution of an integrated development strategy to advance the ... Interface closely with Research/Discovery and Nonclinical team to provide clinical input to ...
Contributes to the development and execution of an integrated development strategy to advance the ... Interface closely with Research/Discovery and Nonclinical team to provide clinical input to ...
Senior Nonclinical Writer (US)
Canton, MI · On-site
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...
Senior Nonclinical Writer (US)
Canton, MI · On-site
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...
Contributes to the development and execution of an integrated development strategy to advance the ... Interface closely with Research/Discovery and Nonclinical team to provide clinical input to ...
Contributes to the development and execution of an integrated development strategy to advance the ... Interface closely with Research/Discovery and Nonclinical team to provide clinical input to ...
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...
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This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...
Bachelor's degree in biological sciences or a related field with 5+ years of relevant R&D ... for nonclinical in vivo studies. * Hands-on experience with in vivo bioluminescence and/or ...
Bachelor's degree in biological sciences or a related field with 5+ years of relevant R&D ... for nonclinical in vivo studies. * Hands-on experience with in vivo bioluminescence and/or ...
Demonstrated knowledge of clinical pharmacology, non-clinical packages, and regulatory requirements supporting global drug development, including first-in-human studies, dose justification ...
Demonstrated knowledge of clinical pharmacology, non-clinical packages, and regulatory requirements supporting global drug development, including first-in-human studies, dose justification ...
This role will report to the Head of Early Clinical Development, Oncology and will have direct ... O.) or non-US equivalent of M.D. degree with relevant hematology and/or oncology in an academic or ...
This role will report to the Head of Early Clinical Development, Oncology and will have direct ... O.) or non-US equivalent of M.D. degree with relevant hematology and/or oncology in an academic or ...
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Head of Methods & AI Integration
Boston, MA • On-site
Full-time
Posted 17 days ago
Takeda Pharmaceuticals rating
7.3
Based on 71 frontline employees who took The Breakroom Quiz
Job description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job DescriptionAbout the role:
The Head of Methods & AI Integration is a senior leadership role within R&D Data and Quantitative Sciences (DQS), reporting to the Head of DQS. This role sits at the intersection of methodological innovation, AI/ML and enterprise-scale deployment within DQS. Unlike traditional functional leadership, it is accountable for translating fragmented AI/ML and quantitative advances into standardized, regulator-ready capabilities adopted consistently across all therapeutic areas and R&D functions.
The Head of Methods & AI Integration will apply a relentless focus on scaling impact - moving innovation from pilot to enterprise deployment - and the integration of data and quantitative science depth with AI/ML and engineering fluency to build a scalable quantitative decision-making backbone for R&D. The role demands credibility with regulators and external scientific communities alongside the operating discipline to govern reproducible, auditable, GxP-ready methods.
Specific areas of accountability for this position include:
Defining, integrating, and scaling advanced data & quantitative science and AI/ML methodologies into decision-grade capabilities across R&D, embedding methodological innovation into clinical development workflows, governance, and decision-making rather than delivering isolated pilots.
Owning the end-to-end lifecycle from innovation to enterprise adoption, transforming fragmented AI and methodological advances into standardized, reusable, regulator-ready capabilities that materially improve decision quality, speed, and development outcomes.
Acting as the critical bridge between innovation, methods, and execution, enabling DQS to deliver a scalable quantitative decision-making backbone across R&D.
Positioning DQS as a global leader in AI-enabled clinical development and decision science through internal enablement and external engagement with regulators, academia, and consortia.
How you will contribute:
Serves as a member of the DQS Leadership Team, influencingfuture strategyandoperationswith DQS and more broadly across the R&D enterprise R&D framing the quantitative decision-making backbone that underpins portfolio-wide decision quality, consistency, and speed.
Define and own the DQS methods strategy spanning data and quantitative science innovation, AI/ML, and decision science, establishing next-generation methodologies for clinical trial design and optimization (e.g., simulation, adaptive designs) and AI-enabled decision-making (e.g., GenAI, causal ML, digital twins, evidence synthesis).
Lead the systematic integration of AI/ML into clinical development workflows, shifting from pilot use to embedded, standardized capabilities delivered as reusable tools, frameworks, playbooks, and decision-support systems.
Own the end-to-end lifecycle (innovation validation deployment scale), ensuring solutions are decision-ready, reproducible, governed, and deployable in GxP/regulated environments, and eliminating "pilot-only" efforts through repeatable scaling pathways.
Embed advanced methods into core R&D decisions - Go/No-Go, trial design and simulation, and portfolio strategy and trade-offs - enabling consistent, transparent, and portfolio-comparable decision frameworks across therapeutic area units (TAUs).
Define and implement the enterprise methods and AI governance framework, including model qualification, regulatory alignment, and standards for reproducibility, documentation, and auditability, driving standardization and reuse to reduce fragmentation and bespoke approaches across programs.
Establish standards for model validation, method qualification, deployment readiness, and lifecycle management that are scientifically rigorous, transparent, and fit for regulatory purpose.
Build and lead a high-impact, multi-disciplinary team across AI/ML methods, advanced data and quantitative science methodology, decision science, and translation/enablement, operating a hub-and-spoke model in partnership with SQS, QPTS, PSPV, and DD&T, etc.
Engage regulators, academia, and consortia to shape methodological and AI standards and advance acceptance of AI-driven approaches in regulated environments, positioning DQS as a global leader in AI-enabled decision science.
Drives impact on development success rates (PTRS), trial efficiency and design optimization, and reduced attrition and development timelines.
Enhances Takeda's external influence on regulatory and scientific standards for AI-enabled clinical development and decision science.
Preferred Qualifications:
PhD in Statistics, Data Science, or other quantitative field with ~15+ years of experience, including extensive leadership in quantitative sciences in pharma/biotech and in AI/ML or advanced analytics in regulated environments.
MS in Statistics, Data Science, or other quantitative field with ~18+ years of equivalent experience, with a proven track record of translating innovation into enterprise-scale capabilities and driving cross-functional transformation across R&D.
Deep expertise in data and quantitative science methodology and in AI/ML and modern analytic approaches, with the technical authority to set and drive functional methods strategy across R&D.
Experience owning accountability for methodology decision-making - selecting, qualifying, and standardizing methods that optimize the likelihood of drug R&D success.
The ability to identify and create the technical and methodological strategic vision and implement long-term innovation aligned with global regulatory and payer expectations, GxP environments, and trends.
Strong command of model validation, governance, and lifecycle management, ensuring methods and AI capabilities are reproducible, auditable, and fit for regulatory purpose at scale across R&D.
The capability to establish external networks and lead strategic DQS and R&D collaborations across industry, government, regulators, and academia to advance acceptance of AI-driven approaches.
Operate with an enterprise mindset, focused on scaling impact rather than isolated innovation.
Create and develop complex, multi-functional methods and AI strategy and mobilize organizations across R&D to adopt it.
Bridge science, technology, and business decision-making, and influence across global, matrixed organizations.
Act as a strong change agent and decision maker driving AI-enabled transformation across R&D.
Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
Boston, MAU.S. Base Salary Range:
$259,000.00 - $407,000.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
For information about our benefits, please click here.
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeJob Exempt
YesIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.What Takeda Pharmaceuticals employees say
Pay
Benefits
Hours and flexibility
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About Takeda Ventures
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Industry
Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
1 - 10 Employees
Headquarters location
San Diego, CA, US