Senior Program Manager

🔥 12 hours ago

🇺🇸 United States – Remote

💵 $66k - $169.4k / year

⏰ Full Time

🟠 Senior

📋 Program Manager

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Eli Lilly and Company

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company is a multinational pharmaceutical company that researches, develops, manufactures, and markets prescription medicines across multiple therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain. Headquartered in Indianapolis, Indiana, Lilly is known for its extensive R&D, clinical development, and global commercialization of biologic and small-molecule drugs. The company focuses on drug discovery, clinical trials, regulatory approvals, and large-scale pharmaceutical manufacturing and distribution.

📋 Description

• Partner with the Global Team Leader and Director of Project Management to support cross-functional matrix teams and project-manage select sub-teams • Develop and continuously maintain assigned portions of detailed, fully cross-functionally integrated program Gantt charts as a company-wide single source of truth • Provide fit-for-purpose summary views for team use and executive management reviews • Identify and manage interdependencies, critical paths, and at-risk activities for program-level scenario planning and risk management • Maintain dashboards to communicate status and track progress • Manage cross-functional team meetings, including scheduling, agendas, presentation materials, minutes, and action-item follow-up • Maintain issue logs and risk registers and ensure timely issue resolution and risk mitigation • Work with cross-functional teams and Finance to develop and update budgets and manage program spend within approved budgets • Manage selected external vendors, including timelines, budgets, MSA/SOW documents, and deliverable integration into program Gantt charts • Support development of Governance and Executive presentations • Support planning and preparation of documents meeting quality standards for Regulatory/Health Authority submissions • Contribute to establishing and refining best practices, processes, and procedures

🎯 Requirements

• BS plus 5+ years of experience in a pharmaceutical/biotech R&D environment, including 3+ years as a project manager or equivalent • Proven expertise in drug development and registration, including early- and late-stage clinical, nonclinical, CMC development, and global regulatory interactions, submissions, and reviews • Strong communication, collaboration, interpersonal, and influencing skills • Excellent analytical skills and expertise in facilitating team decision-making • Competence in decision analysis methodologies and related tools • Expert knowledge of project management principles and practices • Expertise in project management software, such as Smartsheet • Ability to thrive in a fast-paced, dynamic environment • PMP certification highly desired

🏖️ Benefits

• Company bonus depending on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical, dental, vision, and prescription drug benefits • Healthcare and/or dependent day care flexible spending accounts • Life insurance and death benefits • Time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities • Accommodation support for applicants with disabilities