Skip to main content
← Back to Jobs

Clinical Development Director - Oncology

AmgenUnited States🌍 Remote
Full-timeSenior
$275k - $372k
per year
👁️ 0 views📝 0 applicationsPosted 8/18/2026Expires 10/17/2026
Tailor Resume for This JobCheck ATS Score

Get alerts for roles like this

More Clinical Development Director - Oncology roles in United States — straight to your inbox. No account needed.

Applying to this role? Tailor your résumé to this job description in one click, then download it clean — no watermark, no subscription.

Job Description

Career Category Clinical 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.

Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions.

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 Development Director - Oncology What you will do Let’s do this. Let’s change the world.

In this vital role you will support Clinical Development in Prostate cancer.

Supporting the development, execution and communication of the global scientific/medical evidence plan Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program Supporting the development of key scientific external relationships with opinion leaders Participating and providing clinical input into safety and regulatory interactions Provide clinical/scientific input during the development and execution of clinical trials Interpret clinical trial data Participate in safety assessments Participate in interactions with regulatory agencies Author CSRs, publications and regulatory submi

Required Skills

Clinical DevelopmentOncologyClinical TrialsSafety AssessmentsRegulatory InteractionsClinical InputData InterpretationScientific Evidence PlanCross-functional CollaborationMedical RelationshipsPublicationsRegulatory Submissions

The best-paying roles in your field. Every week. Free.

Join 10,000+ professionals getting job alerts and salary insights in their inbox

We respect your privacy. Unsubscribe anytime with one click.