Senior Manager, Business Capability Analyst, Global Regulatory Information Data & Systems
Company websitetakeda.com (Takeda, opens in new tab)
Base salary $137,000 to $215,270
Employer-published annual base salary, USD. Advertised base range in Boston, MA
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationBoston, MA
- WorkplaceWorkplace not stated
- Status at last checkSource accepting applications when checked
- Last checked (1 h ago) · observed since
About this job
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
Objective / Purpose:
The Senior Manager, Business Capability Analyst, Global Regulatory Information Data & Systems serves as a strategic liaison between regulatory business stakeholders and Digital & Technology teams, enabling the successful delivery of regulatory data and system capabilities across the GRIDS portfolio.
This role is responsible for eliciting, shaping, and translating business needs into actionable requirements, while assessing end-to-end process and data impacts. The role ensures that solutions are aligned to regulatory objectives and delivered in a scalable, compliant, and value-driven manner.
Accountabilities:
· Partner with Business System Owners and stakeholders to elicit and document business requirements
· Facilitate workshops to define use cases, scenarios, and regulatory needs
· Assess end-to-end process and data impacts of new capabilities across regulatory functions
· Translate business requirements into functional specifications, user stories, and acceptance criteria
· Collaborate with Digital & Technology teams to support agile delivery and backlog refinement
· Serve as a key interface between business and technical teams to ensure alignment and clarity
· Identify opportunities for process optimization, data quality improvements, and capability advancement
· Support consistent application of business analysis standards, tools, and methodologies
· Contribute to successful implementation and adoption of regulatory system capabilities
Education & Competencies (Technical and Behavioral):
- Education & Experience
- Bachelor’s degree required; advanced degree preferred
- 8–12+ years of business analysis experience in life sciences or regulatory domains
- Experience with regulatory systems (e.g., Veeva RIM)
- Strong understanding of GxP environments and regulatory processes
- Technical Competencies
- Requirements elicitation, documentation, and management
- Translation of business needs into structured technical artifacts
- Understanding of regulatory data models and process flows
- Experience working within Agile or hybrid delivery environments
- Behavioral & Leadership Competencies
- Strong stakeholder management and cross-functional collaboration
- Ability to facilitate alignment between business and technical teams
- Structured thinking and problem-solving
- Clear and effective communication
- Continuous improvement mindset with focus on capability building
- Demonstrates Takeda leadership behaviors through strategic thinking, collaboration, delivery focus, and capability development
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:
$137,000.00 - $215,270.00
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.
Locations
Boston, MAWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full 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.Source: Takeda on Workday · View original posting (opens in new tab)
Pay in context
This role's base floor ($137,000) is above 46% of the 232 Program & Project Management roles in Massachusetts listed on this site; 1 other lists the same floor. Their median floor is $140,000; the middle half runs from $117,596 to $162,200.
Only jobs on this site count, and each one publishes a base salary of $100,000 or more, so this compares six-figure jobs with each other, not with the whole market. Computed Nov 8, 2026.
This listingSenior Manager, Business Capability Analyst, Global Regulatory Information Data & Systems$137,000 to $215,270
Senior Manager, US Medical Ad/Promo Regulatory Review$137,000 to $215,270
Senior Manager/Lead, Contract Management, US Oncology$137,000 to $215,270
Senior Manager, GDO Trial Performance Intelligence and Strategy$137,000 to $215,270
Senior Scientist, High-Throughput In Vitro ADME$137,000 to $215,270
Senior Staff Engineer, Modeling and Data Applications$137,000 to $215,270
Senior Principal Pharmacovigilance Scientist$137,000 to $215,270
Chart as a table
| Role | Published base |
|---|---|
| Senior Manager, Business Capability Analyst, Global Regulatory Information Data & Systems (this listing) | $137,000 - $215,270 |
| Senior Manager, US Medical Ad/Promo Regulatory Review | $137,000 - $215,270 |
| Senior Manager/Lead, Contract Management, US Oncology | $137,000 - $215,270 |
| Senior Manager, GDO Trial Performance Intelligence and Strategy | $137,000 - $215,270 |
| Senior Scientist, High-Throughput In Vitro ADME | $137,000 - $215,270 |
| Senior Staff Engineer, Modeling and Data Applications | $137,000 - $215,270 |
| Senior Principal Pharmacovigilance Scientist | $137,000 - $215,270 |
Observed changes
- First observed on the employer's board
- Began meeting the published-salary criteria
- fields changed
- Observed since
- Employer-stated posting date
- 2026-10-28
Where this pay comes from
Location as the employer wrote it: Boston, MA
$137,000.00 - $215,270.00
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
