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Eli Lilly and Company · 9 hours ago

Associate Director (Supervisor) - North America Trial Capabilities

Indianapolis, IN

Full-time

Onsite

Lead/Staff, Director/Executive

$123K/yr - $180K/yr

5+ years exp

Eli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana, dedicated to discovering life-changing medicines. The Associate Director is responsible for overseeing clinical trial initiation activities, providing leadership and guidance to the team, and ensuring efficient execution of clinical development projects.

BiotechnologyHealth CareMedicalPharmaceutical

No H1B

Responsibilities

Be accountable for establishing, obtaining and exceeding goals for clinical trial initiation for development programs

Lead team through site initiation, maintenance, and close-out activities aligned with local/regional requirements, data privacy requirements and Lilly's global quality standards, including but not limited to budget and contract execution

Craft and implement site activation strategies across the dynamic portfolio

Continually strengthen the customer experience through innovative strategic solutions

Build synergetic relationships with key business partners, maintaining clear communication of progress through the delivery of all clinical site activities

Prioritize work to meet the needs of the portfolio through ensuring flexibility of resources across trial capabilities teams

Influence the sharing of takeaways across the organization and with other cross-functional groups

Partner across Clinical Capabilities to increase efficiency through the use of technology and other advanced resources

Be accountable for inspection readiness at all times through a complete, accurate and readily available Trial Master File

Foster an innovative attitude and create a culture that drives efficiency through enhanced processes, people skills, and shared learning

Recruit, develop, and retain a scientific and operationally capable workforce skilled and knowledgeable in clinical development

Develop a culture that exemplifies diversity, inclusion and innovation and demonstrates judgment-based decision-making

Drive succession management and performance discussions with a constant focus on continued capability development

Effectively manage an agile organization that continuously meets the needs of a changing portfolio

Qualification

Clinical Trial ManagementLeadership SkillsProject ManagementClinical Development KnowledgeRegulated Environment ExperienceSelf-ManagementCommunication SkillsNegotiation SkillsProblem-Solving SkillsOrganizational Skills

Required

Bachelor's degree preferably in a scientific, health related field or in clinical research experience or relevant experience preferred

2+ years managing a team of direct reports

5+ years in a Clinical Trial environment

Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position