Associate Director, Clinical Trial Program Lead At Lilly, we unite caring with discovery to make life better for people around the world.
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Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself.About The Job The purpose of the Associate Director Clinical Delivery Program Lead is to lead the creation and execution of the exploratory and biopharmaceutics clinical development plans at a molecule level, with technical leadership and operational oversight of clinical research trials within the development plan.
The Associate Director Clinical Delivery Program Lead is responsible for the to planning and delivery of the exploratory and biopharmaceutics clinical molecule and submissions milestones on time and on budget throughout the molecule lifecycle, as well as being and is responsible for all aspects of global clinical trial operations within the plan, as the single operational point of contact from trial design through execution and close out, including timeline creation and management, outsourcing plan, vendor management (including direct oversight of the operational deliverables), patient recruitment and retention and budget management.
Dependent on the operational/resource model chosen and influenced by the needs of the clinical development program the Associate Director may be assigned additional trial level management support from internal or external resources.
The will seek knowledge from internal and external sources and use this information to shape development plans and continuous improvement opportunities.
This job description is intended to provide a general overview of the job requirements at the time it was prepared.
The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description.
Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
Scientific and Therapeutic Area Expertise3-years' experience in the pharmaceutical industry with direct experience of managing clinical studies, ideally in exploratory and biopharmaceutics clinical development (5+ year preferred)..
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