Project Manager Clinical Supply Chain

HOW MIGHT YOU DEFY IMAGINATION?

Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Project Manager - Clinical Supply ChainLive

What you will do

Lets do this. Lets change the world. In this pivotal role, you will responsible for leading the global design and set up of end-to-end customized clinical supply chains in support of the assigned clinical programs/studies in a timely, efficient, effective and independent manner.

Responsibilities

• Develop and employ project management techniques to design and set up supply chains for clinical studies. This includes:
• Create and maintain project plans to ensure timely clinical study starts to support first subject enrolled
• Create and maintain study forecast for finished drug products (both Amgen and non-Amgen) in applicable systems to support clinical study start
• Design optimal packaging configuration for finished drug products taking into account protocol requirements and product characteristics.
• Ensure storage and shipping capabilities plus sufficient capacity for finished drug product is available within Amgen supply chain network (both internal and external) to support global study footprint.
• Design cost efficient (re)supply model to distribute finished drug product via applying risk analysis and mitigation strategy.
• Ensure efficient and smooth hand-over to clinical demand and inventory planning team
• Facilitate the phase in phase out strategy for new medicinal product introduction, such as running scenarios, impact on study demand and set up activities for formulation and device introductions
• Performs other functions as assigned

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients.

Basic Qualifications:

• Doctorate OR
• Masters degree and 2 years of experience OR
• Bachelors degree and 4 years of experience OR
• Associates degree and 10 years of experience OR
• High school diploma / GED and 12 years of experience

Preferred Qualifications:

• Knowledge of clinical supply chain management
• Bachelors degree or equivalent in logistics, business administration or life science.
• 5 years relevant working experience, preferably in the biotechnology or pharmaceutical industry, with an in-depth knowledge of supply chain management and clinical research management principles.
• At minimum 5-year experience in project leadership and project management techniques in an international and regulated environment
• General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
• Fluency in English, both verbal and written communication
• Advanced experience in MS Office applications
• Experience in using ERP systems, preferably SAP
• Project Management certification (PMP, IPMA)

Thrive

Some of the vast rewards of working here

As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.

• Full support and career-development resources to expand your skills, enhance your expertise, and improve your potential along your career journey
• A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
• Generous Total Rewards Plancomprising health, finance and wealth, work/life balance, and career benefitswith compensation and benefits rated above 4 stars (out of 5) on Glassdoor

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

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Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Amgen requires all staff in the United States, Puerto Rico and Canada to be vaccinated from COVID 19 as a condition of employment. In accordance with applicable law, Amgen will provide reasonable accommodations to staff members who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to Amgen, its operations, or its staff.