Associate Director leading the execution of complex clinical trials at Lilly. Collaborating with cross-functional teams to deliver quality trial outcomes within scope and budget.
Responsibilities
Independently leads the cross-functional study team in the development and execution of complex clinical trials
Accountable both regionally and globally to deliver clinical milestones on trial(s) with quality, on time, and within scope and budget
Drive to solutions across the molecule/program
Be accountable for trial/regional/program/molecule enrollment strategy and execution from country allocation through Last Patient Entered Treatment (LPET)
Partner with the Regional Operations to achieve regional enrollment goals
Anticipate and resolve complex and key technical operational or business problems with cross-functional study team
Leverage and demonstrate broad understanding of therapeutic, clinical drug development, and process expertise in order to influence study design and program-level decisions considering regional needs
Single point of accountability for the Trial Master File for assigned trials
Ensure inspection readiness of respective clinical trial(s).
Requirements
Bachelor's degree (scientific or health-related field preferred)
5+ years clinical research experience or relevant experience in a scientific or health-related field
Experience with oncology (early phase clinical trial highly preferred)
Experience with radioligand therapy (RLT)
Applied knowledge of project management methodology, processes and tools
Demonstrated ability to lead and work effectively cross-culturally with global colleagues and with TPOs
Be recognized as a leader with demonstrated ability to coach others in process expertise.
Embrace strategic organizational changes and lead others effectively through these, exhibiting flexibility to adjust quickly and effectively to frequent change and altered priorities
Ability to influence without authority
Previous experience working in cross-functional teams/ projects and/or ability to establish and maintain relationships
Strong analytical skills
Proficiency in use of project management tools and techniques (e.g., Critical Chain, Veeva, MS Project, MS Excel, MS PowerPoint, PowerBI)
Benefits
eligibility to participate in a company-sponsored 401(k)
pension
vacation benefits
eligibility for medical, dental, vision and prescription drug benefits
flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
life insurance and death benefits
certain time off and leave of absence benefits
well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
Job title
Associate Director, Clinical Development Trial Lead
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