Takeda

Director Clinical Operations

Takeda • $177K — $278K *
US-AnywhereRemote in Massachusetts, US
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences or equivalent; advanced degree preferred.
  • 12+ years in pharmaceutical industry/clinical research, with 9+ years in clinical study management.
  • Experience in early phase, Phase 2 and 3 studies, as well as global/international programs.
  • Proven leadership and project management skills, with innovative operational approaches.
  • Expertise in global regulatory and compliance for clinical research, including ICH GCP.

Responsibilities

  • Lead and direct execution of clinical programs within a Therapeutic Area Unit.
  • Provide expert counsel for resolution of issues related to assigned programs.
  • Oversee program execution, focusing on quality, budget, and timelines.
  • Ensure compliance with ICH-GCP and Takeda's business objectives.
  • Communicate program status and issues for timely decision-making.
  • Supervise Strategic Partners and vendor selection, ensuring contract compliance.
  • Prepare for inspections and guide operational teams for readiness.

Benefits

  • Remote working flexibility within a supportive company culture.
  • Opportunities for professional development and continued education.
  • Engagement with innovative projects influencing patient outcomes.
  • Collaboration with cross-functional teams and global stakeholders.
Full Job Description
Job Description

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.

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)).

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.


EDUCATION AND EXPERIENCE:
  • 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.


TRAVEL REQUIREMENTS:
  • Requires up to 10% travel, including overnight and international travel to other Takeda sites, strategic partners, and therapeutic area required travel.


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:
Massachusetts - Virtual

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.

For information about our benefits, please click here.

Locations
Massachusetts - Virtual

Worker Type
Employee

Worker Sub-Type
Regular

Time Type
Full time

Job Exempt
Yes

About Takeda

Takeda Pharmaceutical Company Limited is a global pharmaceutical company that develops and markets pharmaceutical products. The company's products are used to treat a wide range of medical conditions, including cardiovascular and metabolic diseases, respiratory diseases, and cancer. Takeda Pharmaceutical Company Limited was founded in 1781 and is headquartered in Tokyo, Japan. The company has operations in more than 80 countries and employs more than 49,000 people worldwide.
Learn more about Takeda
Size
47,347 employees
Market Cap
$48.2 billion
Industry
Founded
1781
5 Year Trend
+15.6%
NASDAQ

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