New · posted Nov 13
Takeda · Pharmaceuticals
Associate Medical Director, Clinical Science – Inflammation TAU
- Cambridge, MA
- On-site
- Full-time
- Director
The role
The Associate Medical Director, Clinical Science, Inflammation is responsible for providing clinical research leadership to ensure the successful strategic implementation of clinical programs. This role involves designing, overseeing, and conducting clinical studies, ensuring compliance with regulatory standards, and contributing to the advancement of medical science.
How you will contribute
- Partner with leadership to translate strategy into executable research plans
- Design, oversee, and conduct clinical studies within assigned therapeutic areas
- Manage individual study budgets and communicate status to stakeholders
- Represent US Medical Clinical Research with external collaborators and investigators
- Identify and drive innovative process improvements with significant organizational impact
- Lead and matrix-manage high-performing study teams
- Provide financial oversight for program/study budgets
What you need
- MD or internationally recognized equivalent plus 3 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned).
- Dermatology is a plus
- Comprehensive understanding of clinical research and medical regulatory processes, capable of leading complex clinical programs
- Expertise in medical science with the ability to provide high-level scientific consultation
- Proficient in regulatory compliance, ensuring all research activities meet required standards
- Skilled in building and maintaining professional relationships to enhance research outcomes
- Advanced ability in data interpretation, particularly of Phase I-III clinical trials
- Leadership skills with experience in mentoring and guiding teams towards achieving scientific and commercial goals
- Effective project management skills, capable of overseeing multiple research initiatives
- Experienced in scientific consulting, providing valuable insights to project teams
- Strong team collaboration skills, promoting an inclusive and productive work environment
- Strategic planning abilities, adept at aligning research activities with broader company objectives
- Problem-solving skills, with a knack for identifying and addressing challenges proactively
- Excellent communication skills, proficient in conveying complex information clearly and persuasively
As a recognized expert within your business or function, you possess comprehensive expertise in your discipline and broad knowledge across related areas. You excel at anticipating internal/external challenges, recommending improvements, and providing leadership and consultative expertise for a specific business, region or function. Your role involves shaping company policies, solving unique, far-reaching problems affecting operations, disciplines, or other business units/functional areas/regions. You frequently interact with equivalent-level managers and customer representatives, conducting briefings and technical meetings. Operating independently, you provide guidance in the most complex situations, lead functional teams or projects, and serve as a best practice/quality resource.
Pay
$198,500 – $311,850 a year
Employer providedU.S. Base Salary Range
$198,500.00 - $311,850.00
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.
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.
Where you'll work
Cambridge, MAOn-siteOpen in Maps (opens in a new tab)
More jobs in Cambridge, MAWorking conditions
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
From the posting
About Takeda
For Location
USA - MA - Cambridge - Binney St
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.
Equal opportunity, accessibility and legal noticesTakeda's statements, word for word
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.
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.
Job intelligence
The context around this role
Live data · November 13, 2026
Salary intelligence
How the pay compares
This role's midpoint is 15% below the US median for Clinical Development roles at this level.
This roleEmployer provided
Director roles in Massachusetts67 roles publishing pay
Director roles in the US216 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $198,500 | — | $311,850 |
| Massachusetts (middle half) | $253,000 | $297,000 | $321,750 |
| All US (middle half) | $254,500 | $300,000 | $335,500 |
This role: Takeda's own published range. Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, November 13, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Development
The general path across 288 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not Takeda's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership10
- Clinical trial conduct6
- GMP and compliance2
- Lab testing and methods1
- Investigations and CAPA1
- Quality systems and risk1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Development work in pharmaceuticals, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- ICHICH E8(R1)(official source, opens in a new tab)General considerations for clinical studies and quality by design in trials
- HHS45 CFR Part 46 (Common Rule)(official source, opens in a new tab)The federal policy for the protection of human research subjects
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
Company hiring pulse
Takeda on Regulatory Jobs
- 68
- Open roles
- 68
- Distinct roles
- 16
- Locations
By discipline
- Clinical26 38%
- Regulatory25 36%
- Quality17 25%
By level
- Director42 61%
- Senior & Principal11 16%
- Manager9 13%
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Associate Medical Director, Clinical Science – Inflammation TAU at Takeda
Open until filled. $199K–$312K a year, employer provided.