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Global CDO TA Executive Director - Eye Health (Remote)

Work from home Full-time role Hiring

Step into a high-impact leadership role as Clinical Development Operations (CDO) Therapeutic Area (TA) Head at Boehringer Ingelheim and take the opportunity to drive innovation and operational excellence across global clinical development programs in the Eye Health TA. In this role, you will act as the strategic bridge between the Therapeutic Area (TA) and Clinical Development Operations (CDO), shaping and accelerating execution through a combination of visionary strategy, digital innovation, and global collaboration. By inspiring teams, influencing industry benchmarks, and fostering strategic partnerships, you will create real value for patients and healthcare systems. This position offers the chance to lead with purpose, delivering operational excellence while making a meaningful impact on a global scale. The CDO TA Head acts as the functional manager for the Clinical Development Operations Lead (CDOL), who is appointed at the program level. In clinical programs where no CDOL is appointed (e.g., early development or programs with few studies), the CDO TA Head assumes the responsibilities of the CDOL. This role is posted in the US and Germany. If you want to apply for the position in the Germany, please use this link: Head of CD&O TA Eye Health As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. Duties & Responsibilities

  • Develop and implement operational strategy to accelerate and optimize clinical development programs within the Therapeutic Area Eye Health. You will aim to exceed industry benchmarks for speed, quality, and value.
  • Oversee governance and execution of clinical programs by reviewing Asset Evidence Plans and Execution Excellence Plans, ensuring alignment with strategic goals and timely delivery.
  • Manage clinical program budgets by planning accurately, monitoring financial performance, and ensuring adherence to target parameters.
  • Lead and support cross-functional teams by acting as the functional manager for Clinical Development Operations Leads (CDOLs) and stepping into the role when needed.
  • Foster strategic partnerships by identifying collaboration opportunities, maintaining high visibility with external stakeholders, and representing Boehringer Ingelheim in governance and alliance meetings.
  • Promote innovation and digital integration by supporting the use of real-world evidence, digital tools, and data-driven planning to enhance study design, site selection, and patient engagement.

Requirements

  • MD or PhD degree is desirable. The minimum is a degree in life sciences with more than fifteen (15) years of experience in clinical development operations.
  • Demonstrate strong leadership and strategic thinking to develop and implement operational strategies that accelerate clinical development and deliver measurable value.
  • Bring deep knowledge of clinical development processes, including study planning, execution, and governance within a therapeutic area. Eye Health experience is a plus.
  • Show financial acumen by managing clinical program budgets accurately and ensuring alignment with financial targets.
  • Possess excellent collaboration and communication skills to engage with internal stakeholders and external partners, including academic institutions, site networks, and alliance partners.
  • Apply digital and data-driven approaches to optimize study design, site selection, and evidence generation using tools like real-world evidence and integrated platforms.Stay current with industry trends and contribute to functional excellence by promoting innovation, compliance, and continuous improvement across clinical operations.

Eligibility Requirements:

  • Must be legally authorized to work in the United States without restriction.

Must be willing to take a drug test and post-offer physical (if required). Must be 18 years of age or older.

Compensation

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