Associate Director Global Clinical Program Management, Obesity - US, Remote

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Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

Associate Director Global Clinical Program Management, Obesity - US, Remote

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What you will do

Let’s do this. Let’s change the world. In this vital role you will coordinate and lead all aspects of the operational strategy, planning, risk assessment and mitigation, and overall delivery of Obesity clinical trial programs globally and support continuous improvement initiatives in Clinical Program Operations (CPO) and Global Development Operations (GDO).

Responsibilities:

• Line Management of Global Trial Managers (GTM)s
• Supports Clinical Program Operations (CPO) Director/Snr Director in the following activities (leads activities in the absence of a director level e.g., on smaller programs):
• Overall delivery of Global clinical program operational strategy, planning, risk assessment and mitigation
• Deliver high-quality clinical trials on time and within budget
• Supports / Leads the Global Clinical Study Team for the allocated program(s)
• Providing clinical operations leadership and expertise on the Evidence Generation Team (EGT) and in development of the Evidence Generation Plan (EGP)
• Provide clinical operations leadership and expertise in EGP delivery through the feasibility and study design process
• Development and oversight of clinical program budgets in collaboration with Therapeutic Area (TA) and Finance
• Managing program-level operational issues and oversight of study team issues
• Maintaining global business relationships cross-functionally and communicating global status of clinical trial programs to senior management
• Representing CPO on process improvement initiatives
• Support CPO resource planning for assigned program(s) in collaboration with Program Resource Management (PRM) and Clinical Program Management Director (CPM-D)

Key Activities:

• Lead all aspects of people management, career development, training and succession planning of GTMs
• Support and mentor GTMs in people management, career development of respective Local Trial Managers (LTMs)
• Supports the Global Clinical Program Management Director/ Snr Director in leading all aspects of the planning and delivery of all studies for the program. Accountable for all studies in the program if no director level present
• Input into product evidence generation plans
• Initiate and support conduct of Country Operational Landscape Assessments and study feasibility with Development Feasibility …