Jobs · Analyst

Director, Clinical Operations, Oncology

BioSpace · United States · 1 wk ago
RemoteRemoteAnalyst$177k–$278k/yrFull-time

About the role

Join us as a Director, Clinical Operations, Oncology based remotely reporting to the Executive Director, Clinical Operations, Oncology. 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.

Responsibilities

  • 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)).
  • 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.

Qualifications

  • Bachelor’s Degree or international equivalent required, Life Sciences preferred.
  • Advanced degree is highly desirable.
  • 12 or more years’ experience in pharmaceutical industry, including 9 or more years in clinical study management.
  • Experience must include early phase experience or Phase 2 and 3 studies and global/international programs.
  • Oncology experience is required.
  • 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.
  • Comfortable with ambiguity.
  • Support a culture of continual improvement and innovation; promote knowledge sharing.

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