New · posted Oct 31
Takeda · Pharmaceuticals
Director, Clinical Operations
- Remote, Massachusetts
- Remote
- Full-time
- Director
The role
Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as a Director, Clinical Operations based remotely reporting to the Senior Director, Clinical Operations.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to work towards their potential through life-changing work. We offer stimulating careers, and work toward excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to provide Better Health and a Brighter Future to people around the world.
Here, you will be a necessary contributor to our inspiring, bold mission.
GOALS
- Lead and direct the execution of multiple clinical program(s) within a Therapeutic Area Unit (TAU).
- Responsible for line management and provides expert counsel for issue resolution, including programs assigned to other staff, when required.
- Provide Clinical Operations leadership under the direction of the Senior Director, Clinical Operations:
- Accountable for the overall execution of the assigned clinical program(s) with focus on quality, budget and timelines.
- Accountable for the oversight of Strategic Partners and other vendors to meet Takeda’s obligations described in ICH-GCP and Takeda’s business objectives.
The assigned clinical program(s) will be large, complex, high risk and/or of business importance to Takeda or potentially a suite of programs, requiring multi-functional leadership experience and skills to achieve program goals. If a single program is assigned, the program will typically be significant in scope (e.g., multiple independent indications with individual Clinical Sub Teams (CSTs)).
What you need
- Bachelor’s Degree or international equivalent required, Life Sciences preferred. Advanced degree is highly desirable.
- 12 or more years’ experience in pharmaceutical industry and/or clinical research organization, including 9+ years clinical study management. Experience must include early phase experience or Phase 2 and 3 studies and global/international programs.
- Experience in more than one therapeutic area and in line management is advantageous.
- Demonstrated excellence in leadership and project/program management, including innovative operations approaches to achieving program goals.
- Expertise in global regulatory and compliance requirements for clinical research, including but not limited to US CFR, EU CTD, and ICH GCP. Awareness of local country requirements is also required.
- Supervisory experience.
- Demonstrated excellence in project/program management and matrix leadership.
- Excellent teamwork, organizational, interpersonal, and problem-solving skills.
- Fluent business English (oral and written).
- Able to influence without authority.
- Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo.
- Pragmatic and willing to drive and support change.
- Is comfortable with ambiguity.
- Support a culture of continual improvement and innovation; promote knowledge sharing.
ACCOUNTABILITIES
- Oversee COPLs assigned to represent Clinical Operations as members of the Global Program Team (GPT) and/or CST, working closely with GPT Leadership to ensure program objectives are met.
- Represent Clinical Operations for assigned program(s) in issue escalation/awareness with senior management, e.g. functional or regional executive staff, PRC, alliance governance committees.
- Contribute to the Clinical Development Plan(s) and associated operational strategy, in support of the Asset Strategy.
- Accountable for program budget planning and external spend related to program execution and works closely with Global Program Management, and Finance to ensure financial accuracy.
- Ensures communication of program status, cost and issues to inform timely decision-making by senior management.
- Oversight of Strategic Partners/CRO/vendor selection, budget and contract negotiation, and proper supervision of performance for all activities assigned to a Strategic Partner/CRO/vendor for assigned program(s), including escalation of issues to and participation in governance committees; accountable for operational risk management strategy in collaboration with Strategic Partners.
- Accountable for inspection readiness and provides appropriate guidance to COPLs/COMs in support of inspection activities
- Collaborates with and is responsible to the Senior Director, Clinical Operations to ensure adequate clinical operations resources are assigned to program(s).
- Demonstrate advanced Takeda Leadership Behaviors and act as a role model for Takeda´s values.
- Recognized as a clinical operations expert by other functions and ability to represent and lead cross functional initiatives.
- May participate in Business Development/in-licensing/alliances evaluations by providing operational due diligence.
- Able to assist in role of Senior Director, Clinical Operations as required.
TRAVEL REQUIREMENTS
- Requires up to 10% travel, including overnight and international travel to other Takeda sites, strategic partners, and therapeutic area required travel.
Pay
$177,000 – $278,080 a year
Employer providedU.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.
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.
Working conditions
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
From the posting
About Takeda
For Location
Massachusetts - Virtual
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 · October 31, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% below the US median for Clinical Operations roles at this level.
This roleEmployer provided
Director roles in the US20 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $177,000 | — | $278,080 |
| All US (middle half) | $216,250 | $233,000 | $244,000 |
This role: Takeda's own published range. Comparisons: the base pay employers published on open Clinical Operations roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Operations
The general path across 42 open Clinical Operations roles on Regulatory Jobs, with the titles they carry most. Not Takeda's own promotion track.
Career resources on Clinical Operations
Skills DNA
What this role leans on
How many of the posting's 36 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership13
- Clinical trial conduct4
- GMP and compliance3
- Regulatory submissions1
- Quality systems and risk1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
- ICHICH E6 good clinical practice(official source, opens in a new tab)The international standard for the conduct of clinical trials
- FDAeCTD(official source, opens in a new tab)The electronic Common Technical Document format for submissions
Company hiring pulse
Takeda on Regulatory Jobs
- 64
- Open roles
- 61
- Distinct roles
- 16
- Locations
By discipline
- Regulatory24 38%
- Clinical21 33%
- Quality18 28%
By level
- Director37 58%
- Senior & Principal12 19%
- Manager9 14%
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Director, Clinical Operations at Takeda
Open until filled. $177K–$278K a year, employer provided.