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Seven years of experience in clinical research/drug development, including the design and implementation of large global clinical trials. In addition to his/her management and focused administrative responsibilities, the Associate Vice President – Medical Development drives strategic planning and, with operations teams and management, oversees the clinical research and overall medical support activities of the group.
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Good Clinical Practices (GCPs), company standards, Lilly policies and procedures, company integrity agreements as applicable, and the Principles of Medical Research and are aligned with the medical vision.
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The Director/Associate Director of CCSI is focused on delivering the implementation of clinical capabilities including but not limited to mobile health care, telemedicine, virtual trial orchestration, recruitment & retention, new site models, central clinical services, mobile research, community engagement, clinical supplies, kitting and/or digital devices.
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Oversight of clinical planning, budgeting, and execution •Responsible for affiliate evaluation and input into clinical planning and contribution to clinical trials and communicates research needs to global Development team, Health Outcomes and Pricing, Reimbursement & Access (PRA) teams to ensure registration and post-registration clinical programs meet the needs of local/regional customers.
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The Principal Software Engineer will play a pivotal role in building transformative gen AI platforms and products across the entire Lilly value chain: drug discovery, research, manufacturing, go-to-market, and general knowledge work.
$121,500 - $195,800 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
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