Clinical Quality Senior Manager

Career Category

Job Description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Clinical Quality Senior Manager

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What you will do

Let’s do this! Let’s change the world! In this vital role you will be a team member on one of the Therapeutic Area (TA) Quality teams, which include Oncology, General Medicine, Rare Disease, and Inflammation/ Biosimilars, and you will report to one of the TA Quality Leads within Clinical & Research Quality (CRQ). As a Senior Manager you will provide proactive, end to end quality oversight through various methods of risk-based quality management activities, including quality by design and real-time analysis of quality data/metrics.

In this important role, you will develop deep knowledge of the TA’s clinical trials and provide oversight and quality management of critical data and processes for global and local study teams and all clinical trial sites who participate in Amgen sponsored trials. In addition, you will support the management of quality and compliance for specific regions, including clinical trial sites and vendors who work within those regions. The TA

Responsibilities

• Review clinical trial protocols ensuring simplification, application of lessons learned, and identification of critical data and processes

• Provide quality oversight for the Risk Assessment Categorization Tool (RACT) for each trial to ensure the proper identification, prioritization, and mitigation of risks to critical data and processes and patient safety, welfare and rights

• Provide oversight for the development and implementation of Quality Plans

• Establish Regional expertise to ensure quality and compliance to local regulations

• Support TA-specific data integrity, including technologies for data collection and measurement …