Senior Director, Investigator Engagement Lead

hace 4 días

Ciudad de México, Ciudad de México Eli Lilly and Company A tiempo completo
Job Title: Senior Director, Investigator Engagement

At Eli Lilly and Company, we are committed to making life better for people around the world. We are a global healthcare leader with a rich history of innovation and a passion for improving human health. Our employees work together to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.

Job Summary:

We are seeking a highly skilled and experienced Senior Director, Investigator Engagement to join our team. This role will be responsible for ensuring high-quality interactions with, and timely robust performance of, global clinical trial sites within an assigned therapeutic area and region. The successful candidate will effectively leverage and oversee regional vendor performance of delegated responsibilities, identify and investigate issues, and drive resolution. This role will also provide leadership in committing and delivering to clinical trial recruitment targets that enable industry-leading cost and cycle time performance metrics.

Key Responsibilities:
  • Responsible for clinical site / Investigator qualification and recruitment performance
  • Deliver global enrollment commitments across the portfolio of work within a therapeutic area(s) and region(s)
  • Ensure productive relationships with investigator sites
  • Maintain awareness of global regulatory requirements and ensure activities are performed according to established guidelines, best practices, and in compliance with all appropriate laws
  • Responsible for appropriate integration, delivery, oversight, and issue mitigation/resolution of comprehensive site monitoring activities within a region and integrated across regions
  • Ensure on-time delivery of data base locks, and inspection readiness within a therapeutic area(s) and region(s)
Organizational Leadership:
  • Support flexibility of resources across therapeutic areas and geographies, while aligning to deliver on company portfolio priorities
  • Responsible for the development and implementation of applicable site risk plans to ensure delivery of clinical trial enrollment commitments and data base locks
  • Serve as liaison between clinical trial sites, third-party vendors, and Lilly
  • Function as the global Investigator engagement point of contact for an assigned therapeutic area, as well as the primary Investigator engagement leader within a specified geography
  • Identify and ensure shared learning across the Investigator engagement organization and with other CDO functional groups
  • Enable a culture of continuous improvement to drive efficiency through therapeutic area knowledge, process improvement, quality, and risk management capabilities, people knowledge, and clinical development expertise, and shared learning
  • Drive to a culture of high quality and inspection readiness, as well as consistent utilization of data to inform decisions
People Management and Development:
  • Recruit, develop, and retain a scientific and technically capable workforce with clinical development and therapeutic knowledge necessary to effectively interact with clinical investigative sites within an assigned geography
  • Effectively manage and coordinate an agile organization that continuously adapts to meet the needs of a changing portfolio
  • Manage a diverse organization that fosters inclusion and innovation
  • Develop a talent base that demonstrates judgment-based decision making, and provides leadership in clinical delivery
Requirements:
  • Bachelor's degree and minimum of 10 years of experience in the pharmaceutical industry and clinical research
  • 3-5 years prior supervisory experience or equivalent
  • Experience in, and/or leading different groups in drug development
  • Broad understanding of pharmaceutical drug development process and experience in the planning and conduct of clinical research
Preferred Qualifications:
  • Bachelor's degree or Advanced degree (e.g. MSc, PhD) in a scientific or health care field
  • Prior experience supervising an organization
  • International or regional clinical operations experience
  • Experience working across functions and affiliates
  • Strong interpersonal skills, including capability to engage in professional relationship building and networking
  • Proven ability to influence cross-functionally without direct authority
  • Proven ability to develop diverse organizational talent
  • Ability to represent positions on difficult business issues

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