Senior Global Program Manager

🕒 October 6

🇺🇸 United States – Remote

💵 $141.8k - $191.9k / year

⏰ Full Time

🟠 Senior

📋 Program Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 29%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Open for 37 days.
• Jobs at this company usually fill in 21 days.
• Reposted 2 times.

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Amgen

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1980

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

💰 $28.5G Post-IPO Debt on 2022-12

Healthcare • Biotechnology • Pharmaceuticals

Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.

📋 Description

• Serve as a strategic partner to Product Team leaders in achieving the program’s strategic vision • Drive development, creation, and implementation of high-quality global coordinated cross-functional project plans • Support cross-functional drug development and commercialization activities for pipeline or inline products • Lead and/or participate in special department, cross-functional, or team projects • Drive the Evidence Generation Team and translate the Target Product Profile and program strategy into an integrated evidence-generation plan • Coordinate execution across Clinical Development and Operations, Regulatory Affairs, Safety, Biostatistics, Clinical Pharmacology, Medical Affairs, Health Economics and Outcomes Research, and other functions • Connect evidence generation and regulatory milestones with global brand planning, access strategy, launch readiness, and lifecycle opportunities • Integrate Evidence Generation Team plans, decisions, risks, and deliverables into broader indication strategy and governance roadmap • Frame decisions, identify interdependencies and critical-path activities, prepare governance recommendations, and drive accountability for milestones, risks, resources, and follow-through • Develop integrated cross-functional plans aligned with overall program strategy • Facilitate resource planning, financial and capacity assessments • Conduct risk management and scenario planning and develop contingency or mitigation plans • Coordinate activities with external business partners and alliances • Drive team effectiveness, integrated evidence strategy, Clinical Development Plan execution, and delivery of clinical and nonclinical data packages • Align evidence-generation activities and development milestones with brand strategy, payer and access needs, launch planning, and lifecycle management • Structure complex cross-functional discussions and prepare scenarios and recommendations for governance and senior leadership review • Maintain an integrated view of program milestones, risks, assumptions, resources, budgets, and functional commitments • Promote effective operating practices across global matrix teams • Drive annual Work Package Team goals and input to the Global Product Strategy • Document issues, decisions, and action items • Identify and escalate cross-functional project issues to the Global Program Manager or Work Package Team Lead

🎯 Requirements

• Doctorate degree and 2 years of Relevant experience OR Master’s degree and 4 years of Relevant experience OR Bachelor’s degree and 6 years of Relevant experience OR Associate’s degree and 10 years of Relevant experience OR High school diploma / GED and 12 years of Relevant experience • Drug development experience including deep experience in one or more core drug development and commercialization functions • Experience leading teams through governance process • Program and project management skills in a healthcare-related environment • Experience operationalizing strategic initiatives, including cross-functional strategic planning and development of integrated plans • Emotional intelligence skills including influencing without authority and navigating within a matrix environment • Experience using Project Management tools, methodologies, practices and infrastructure in the Biopharmaceutical Industry • Experience supporting late-stage drug development, evidence generation, regulatory submission and approval, global launch planning, and/or lifecycle management for a pipeline or inline biopharmaceutical product • Demonstrated experience partnering with development and commercial leaders to lead or enable cross-functional teams • Working knowledge of the end-to-end biopharmaceutical lifecycle and related functional interdependencies • Ability to synthesize scientific, operational, regulatory, financial, access, and commercial inputs into integrated plans and decision-ready recommendations • Sponsorship for this role is not guaranteed

🏖️ Benefits

• A comprehensive employee benefits package • Retirement and Savings Plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • Discretionary annual bonus program • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible • Career development opportunities • Work/life balance

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