Senior Program Manager, Medical Product Development

🔥 1 hour ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $160k - $215k / year

⏰ Full Time

🟠 Senior

📋 Program Manager

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RTI International

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1958

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

RTI International is an independent nonprofit research institute dedicated to improving the human condition through science-based solutions in climate, education, health, and equity. The institute engages in multidisciplinary research spanning diverse areas such as health care, international development, environmental sciences, and social and economic justice. RTI International collaborates with a wide range of partners including governments, businesses, universities, and non-profit organizations to conduct research and provide technical services. It aims to impact global wellbeing by leveraging expertise in fields such as climate change solutions, education reform, public health, food security, and more. RTI International also emphasizes corporate responsibility, sustainability, and commitment to quality and ethics in its operations.

📋 Description

• Manage a portfolio of concurrent drug, biologic, medical device, diagnostic, and combination product development projects • Align scientific objectives, project activities, timelines, resources, and budgets • Define critical studies, tasks, deliverables, milestones, and dependencies with multidisciplinary teams • Develop and maintain project plans, track progress, and ensure accountability • Identify technical and operational risks and coordinate mitigation strategies • Provide judgment on project priorities and execution and escalate issues when needed • Support transition of program responsibilities through knowledge transfer, documentation, and stakeholder continuity • Plan development activities and finalize study protocols and procedures with investigators, scientists, CRO staff, and consultants • Coordinate scientific, technical, regulatory, manufacturing, and commercialization contributions • Facilitate activities across participating organizations and manage interdependencies • Monitor external partner deliverables and resolve quality, schedule, or development issues • Build relationships with clients, investigators, technical experts, and external service providers • Maintain communication across project teams, clients, and stakeholders • Lead project meetings, document decisions, and track action items • Research, synthesize, and summarize scientific and program information for requests, proposals, reports, presentations, and meetings • Communicate project status, risks, budget considerations, and required decisions • Help develop and track project budgets and coordinate adjustments • Manage conference calls, meetings, travel, and other logistics • Support technology scouting and ecosystem mapping for AI trends and strategic investment and partnership decisions • Establish success metrics and feedback loops for AI adoption, tracking adoption, value realization, and readiness • Promote responsible AI deployment, including human-in-the-loop validation, risk-aware experimentation, and governance alignment

🎯 Requirements

• Bachelor’s degree in a relevant scientific, engineering, or related field with 20 or more years of experience in medical device or therapeutic product development activities; or a master’s degree with 15 or more years of experience; or a PhD with 12 or more years of experience • Experience developing therapeutics, medical devices, diagnostics, or combination products • Ability to plan and coordinate complex development activities and manage multiple projects or competing priorities simultaneously • Excellent oral and written communication skills • Ability to synthesize scientific and technical information and communicate it clearly to varied audiences • Strong interpersonal skills and ability to work successfully in multidisciplinary teams and across organizational boundaries • Strong organizational skills, attention to detail, and consistent follow-through • Proficiency in Microsoft Word, Excel, PowerPoint, and Microsoft Project • Legally authorized to work in the United States • Must not require sponsorship for employment visa status, now or in the future • Preferred: Experience managing NIH-funded translational research or product development programs • Preferred: Experience in preclinical and clinical product development • Preferred: Experience coordinating CROs, consultants, or other external development partners • Preferred: Familiarity with chemistry, manufacturing, and controls (CMC) • Preferred: Experience with technical or scientific writing • Preferred: Experience supporting program transitions, transferring institutional knowledge, or assuming responsibility for established project portfolios

🏖️ Benefits

• Competitive base salary • Generous paid time off policy • Merit-based annual increases • Bonus opportunities • Robust recognition program • Health insurance • Dental insurance • Life insurance • Short-term disability insurance • Long-term disability insurance • Retirement savings program such as a 401(k) plan • Paid parental leave for all parents • Financial assistance with adoption expenses • Financial assistance with infertility treatments • Financial reimbursement for education and developmental opportunities • Employee assistance program • Other offerings supporting a healthy work-life balance

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