Associate Director, Clinical Trial Manufacturing and Operations

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work 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. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$118,500 - $173,800

Position Brand Description:

The Clinical Trial (CT) Manufacturing organization is responsible for the on-time delivery of drug product in support of clinical trials (Phase 1 through 4) as well as the associated technical information deliverables in support of regulatory submission. CT Manufacturing is accomplished either externally at approved, qualified External Contract Manufacturing sites, both in the US and OUS, or internally at Lilly manufacturing facilities. The CT Manufacturing organization has responsibility for both the technical and operational components of drug product supply. The Associate Director, CT Manufacturing and Operations has accountability for the leadership, supervision, and development of the team members. The team includes NDP Material Coordinators, Plant Planners and Principal Scientist (CT Mfg Tech Reps). The team provides manufacturing and operational support such as manufacturing site planning, manufacturing oversight and issue resolution, purchase requisition management and logistic coordination for physical material movement, for the assets in the portfolio in all phases of drug development.In addition, this role is expected to be an authority and champion for Operational Excellence