Clinical Research Medical Director, Thoracic Oncology

Career Category

Clinical Development

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 Research Medical Direc

 

What you will do

Let’s do this. Let’s change the world. The Oncology Therapeutic Area within Global Development is rapidly growing and in this vital role you will have an opportunity to shape this Therapeutic Area. This role will report directly to the Global Development Lead for the Program. The position may be US in-person or remote.

 

Responsibilities:

 

•     Serve as non small cell lung cancer clinical expert to provide clinical/scientific knowledge into the development, delivery and communication of the global scientific/medical evidence plan for the indication

•     Serve as the medical monitor on key clinical trials in lung oncology

•     Support cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program

•     Participate and provide clinical input into safety and regulatory interactions

•     Interpret and communicate clinical trial data

•     Author CSRs, publications, and regulatory submissions

•     Develop key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by GDL

•     Identify new clinical research opportunities

•     Support in-licensing and out-licensing activities and partner relationships

•     Support product lifecycle management for new indications as directed by the Global Development Lead

Provide clinical content input to materials to be used in Scientific Affairs as well