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Study Design Lead Jobs (NOW HIRING)

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Mechanical BIM Design Lead (Power/Hydropower) HDR is looking for a Mechanical BIM Design Lead to ... studies for new power generation projects. They will work with a multi-discipline group of ...

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Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

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Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

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Product Design Lead

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Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

Lead + Grow McAdams' NCDOT Design Team At McAdams, we invest in growth-minded leaders who are eager ... Proven success winning and delivering work for NCDOT units, including Feasibility Studies ...

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Study Design Lead information

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$36K

$81.2K

$156K

How much do study design lead jobs pay per year?

As of Jun 23, 2026, the average yearly pay for study design lead in the United States is $81,196.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,000.00 and $90,000.00 per year, depending on experience, location, and employer.

Can you be a CRA with no experience?

A Clinical Research Associate (CRA) typically requires prior experience in clinical trials, monitoring, or related healthcare fields. Entry-level CRA positions may be available for candidates with strong organizational skills and relevant certifications, but most roles prefer candidates with some industry experience or training in Good Clinical Practice (GCP) guidelines.

What are Study Design Leads?

Study Design Leads are professionals responsible for planning, coordinating, and overseeing the design of research studies, typically in clinical, pharmaceutical, or academic settings. They work closely with cross-functional teams to develop study protocols, ensure regulatory compliance, and optimize study methodologies. Their goal is to ensure that studies are scientifically sound, feasible, and meet ethical standards. Study Design Leads play a critical role in the success of research projects by guiding the study from conception through to execution.

What jobs pay 2000 a day?

High-paying jobs that can pay around $2,000 a day typically include specialized roles such as senior consultants, surgeons, corporate lawyers, or executive-level positions. These roles often require advanced skills, extensive experience, and sometimes professional certifications, and they may involve project-based work or high-demand expertise.

What is the highest paying job in design?

In design fields, user experience (UX) directors and creative directors often have the highest salaries, especially in large organizations or tech companies. These roles typically require extensive experience, leadership skills, and proficiency with design tools and user research methods.

What is the role of a design lead?

A study design lead is responsible for developing and overseeing the methodology of research studies, ensuring they are scientifically sound and aligned with project goals. They coordinate with cross-functional teams, analyze data, and ensure compliance with regulatory standards, often utilizing statistical tools and research protocols.

How does a Study Design Lead typically collaborate with cross-functional teams during the planning phase of a clinical trial?

A Study Design Lead works closely with cross-functional teams such as clinical operations, biostatistics, data management, regulatory affairs, and medical writing to ensure that study protocols are scientifically sound and operationally feasible. They facilitate communication between departments to align objectives, address potential challenges, and incorporate regulatory and ethical considerations early in the process. This collaborative approach helps streamline trial execution and ensures that the study design supports clear endpoints and data collection requirements.

What are the key skills and qualifications needed to thrive as a Study Design Lead, and why are they important?

To thrive as a Study Design Lead, you need a strong background in clinical research, biostatistics, and study protocol development, typically supported by an advanced degree in life sciences or a related field. Proficiency with clinical trial management systems (CTMS), statistical software (such as SAS or R), and familiarity with regulatory requirements like ICH-GCP are essential. Excellent project management, communication, and leadership skills set standout candidates apart, enabling effective collaboration across multidisciplinary teams. These skills ensure that studies are scientifically robust, compliant, and efficiently executed, ultimately supporting successful research outcomes.
More about Study Design Lead jobs
Infographic showing various Study Design Lead job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 88% Full Time, and 11% Part Time. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $81,196 per year, or $39 per hour.
AIRx Director, Computational & AI Biologics Design Lead

AIRx Director, Computational & AI Biologics Design Lead

Takeda Pharmaceutical

Cambridge, MA • On-site, Remote

Full-time

Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

58th of 71 rated pharmaceutical


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 Description

Director, Computational & AI Biologics Design Lead

Takeda Research is constructing a Lab of Tomorrow built on AI, automation, new ways of working, and talent with the singular vision of delivering differentiated medicines to the clinic at speed and cost. To catalyze these efforts, Takeda is creating two complementary units: AI Research Accelerator (AIRx) and Discovery Automation & Robotics (DAR).

AIRx will have a group of a dedicated group of experienced biologic drug hunters with the autonomy of a biotech and the resources of a leading pharmaceutical company. It is designed to incubate the future AI-powered operating models for large molecule discovery and deliver candidates to the clinic at industry leading speed and success rates.

Purpose

Reporting to the Head of AIRx, the Computational & AI Biologics Design Lead sits at the scientific heart of the Takeda Boston (TBOS) Large Molecule Pod. As part of the AIRx team, this role serves as a strategic computational leader, driving in silico biologics design and shaping how AI-enabled biologics discovery is executed for select programs.  This role drives in silico biologics design, applies generative AI and structure-informed methods to antibody and large-molecule programs, and connects Takeda’s internal AI/ML platform capabilities to the day-to-day decisions of a fast-moving drug-hunting team.

In addition, the role defines decision frameworks and scientific standards that influence candidate prioritization, progression, and overall portfolio direction.  Proposals from this role directly shape what gets engineered, what gets deprioritized, and what ultimately reaches the clinic. The role is deeply hands-on, with a mandate to operate with urgency and independence while remaining tightly integrated with biology, protein engineering, and translational science colleagues across the pod.

Key Accountabilities

1. In Silico Biologics Design for Pod Programs

  • Define and drive the computational design strategy across the pod’s large-molecule programs,  including antibody, VHH, and multispecific or fusion formats, from early format selection through lead optimization.
  • Design and prioritize molecular candidates using generative AI/ML and computational modeling approaches
  • Serve as a scientific advisor to pod leadership on computational design decisions, influencing program direction and key trade-offs
  • Partner closely with the Biologics Discovery Lead to translate computational proposals into testable engineering priorities; challenge and be challenged on scientific assumptions in equal measure.
  • Integrate structural biology data into design strategies to inform format selection, epitope targeting, and interface optimization.
  • Oversee virtual screening, binding affinity prediction, and developability risk assessment for candidate sequences; provide ranked shortlists with quantified uncertainty to the pod.
  • Establish and improve approaches to accelerate lead optimization by compressing DMTA cycles through AI-guided design, with the goal of achieving the target candidate profile in fewer rounds.
  • Collaborate with translational and DMPK scientists to model PK/PD behavior, TMDD, and species cross-reactivity in silico, informing study design and reducing in vivo cycle time.

2. AI/ML Platform Interface and Data Strategy

  • Serve as the pod’s primary computational interface to Takeda’s AI/ML research platform; evaluate and benchmark new AI design tools against the pod’s specific biologics modalities and program needs.
  • Define and steward data requirements for AI model training within the pod: structure data return from experimental campaigns, annotation standards, and integration with Takeda’s data infrastructure.
  • Contribute to building and curating AI/ML training datasets from pod experimental outputs to enable continuous model improvement.
  • Guide development and refinement of computational workflows to enable pod scalability, speed and reproducibility across the DMTA cycle; document methods to support cross-pod learning.

3. Pod Integration and Scientific Operations

  • Act as a hands-on computational authority within pod governance: prepare and present in silico analyses for PRC reviews, design review boards, and candidate declaration milestones.
  • Ensure computational requirements are integrated early in external experimental campaigns to maximize data return value.
  • Interface with Takeda’s discovery automation capabilities to define assay and data readout specifications for pod programs entering automated workflows when applicable.

4. Scientific Leadership and External Engagement

  • Maintain deep subject-matter expertise by staying current with advances in AI for biologics design and structure prediction; translate emerging capabilities into actionable proposals for the pod.
  • Identify and translate relevant external innovations into opportunities that enhance pod capabilities and programs
  • Represent Takeda’s computational biologics capabilities in interactions with external partners, at conferences, and in the scientific community; contribute to publications and IP filings as appropriate.
  • Provide scientific mentorship within the AIRx context and help shape computational biologics practices across the broader research organization.

Qualifications & Competencies

Expected Requirements:

  • PhD in Computational Biology, Bioinformatics, Structural Biology, Computer Science, or a closely related discipline.
  • 10+ years of drug discovery experience with a demonstrated track record of computational impact on large-molecule or biologics programs; industry experience strongly preferred.
  • Deep expertise in antibody and protein sequence, structure, and function modeling, with proficiency in generative or predictive AI frameworks applied to biologics design.
  • Broad proficiency in computational tools relevant to biologics, spanning structural analysis, molecular simulation, developability prediction, and bioinformatics.
  • Strong coding skills (Python required); experience building and deploying ML models in a drug discovery context; familiarity with cloud-based compute and MLOps practices.
  • Demonstrated ability to operate as both a technical individual contributor and a cross-functional scientific partner in a fast-paced, program-driven environment.
  • Versatile communicator: able to present complex computational findings to biologists, clinical scientists, and senior leadership with clarity and scientific rigor.

Preferred

  • Experience with multispecific antibody formats and the associated engineering, developability, and PK/PD considerations.
  • Experience integrating physics-based modeling with deep learning approaches to improve prediction accuracy and generalization.
  • Prior experience defining data requirements and governance for AI/ML platform development across multiple programs or sites.
  • Experience operating within or alongside an external AI design partner environment, including co-design workflows and campaign-level data return.
  • Track record of contributing to IND-enabling programs; familiarity with candidate declaration criteria and biologics CMC considerations.

ADDITIONAL INFORMATION

  • The position will be based in Cambridge, MA.  This position is currently classified as “hybrid” by Takeda’s Hybrid and Remote Work policy

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, MA

U.S. Base Salary Range:

$177,000.00 - $278,080.00


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. 

U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. 

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 Type

Job 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.

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