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Senior Vice President, Global Study Operations

2 months ago

Oklahoma City, Oklahoma, United States Takeda Full time

Introduction:

At Takeda, we are dedicated to fostering a patient-centric environment that empowers our employees to reach their full potential. We invite you to explore the opportunity to join our team as the Senior Vice President, Global Study Operations, a role that reports directly to the Head of Global Clinical Development Operations.

About Us:

As a leader in the pharmaceutical sector, Takeda is committed to innovation and excellence in research and development. Our culture is built on values that prioritize collaboration and inclusivity, driving us to deliver better health outcomes for patients worldwide.

Key Responsibilities:

  • Provide strategic direction and oversight for the Global Clinical Operations Study Management team, ensuring effective management across all therapeutic domains.
  • Lead a dedicated team focused on Early Clinical Operations, enhancing our operational capabilities.
  • Implement and manage a flexible resource allocation model to optimize study management.
  • Facilitate training and development programs for Clinical Operations Managers and Clinical Trial Associates.
  • Enhance site training initiatives to strengthen Takeda's presence within the external investigator community.
  • Ensure the successful planning, execution, and conclusion of clinical trials across diverse therapeutic areas and geographical regions.
  • Drive operational excellence and maintain high standards of quality in clinical trial management.
  • Promote a culture of collaboration, innovation, and continuous improvement within the Study Management team and across cross-functional teams.

Accountabilities:

  • Lead and mentor a team of Clinical Operations Managers and Clinical Trial Associates, establishing a clear vision and direction for the function.
  • Oversee the upskilling of team members and implement innovative working methods, integrating data and digital solutions.
  • Guide and ensure alignment of resourcing, planning, execution, and completion of clinical trials with overall program strategies.
  • Collaborate with relevant departments to operationalize a comprehensive training strategy aimed at enhancing capabilities and standardization.
  • Ensure adherence to regulatory standards, industry practices, and internal policies throughout the clinical trial lifecycle.
  • Work alongside cross-functional teams to guarantee seamless execution of clinical trials.
  • Monitor and address risks and challenges related to study management, escalating issues as necessary.
  • Build robust relationships with external vendors and partners involved in clinical trial execution.
  • Drive initiatives for continuous improvement to enhance operational efficiency and quality in study management.

Qualifications:

  • Bachelor's degree or equivalent in Life Sciences; advanced degree preferred.
  • 15+ years of relevant clinical development and operations experience, with a minimum of 5 years in a global leadership capacity.
  • Global experience is essential, with a proven ability to collaborate with teams across various locations.
  • Demonstrated success in leading training strategies and driving standardization across clinical trials.
  • Extensive operational experience in pharmaceutical drug development, with significant exposure to clinical development across multiple therapeutic areas.
  • Proven track record in leading and developing large, diverse, globally dispersed teams, particularly through transformational changes.
  • Strong understanding of the pharmaceutical industry and healthcare business acumen.

Compensation and Benefits:

At Takeda, we recognize the importance of fair compensation and strive for transparency in our pay practices. We offer competitive salaries and a comprehensive benefits package to support our employees' well-being.

Diversity and Inclusion:

Takeda is committed to creating a diverse workforce and providing equal employment opportunities to all employees and applicants, ensuring a workplace free from discrimination.

Work Environment:

This position is designed to be performed in a virtual setting, allowing for flexibility and work-life balance.