Clinical Research Medical Director, Endocrinology/Obesity/Diabetes, US - Remote

Amgen; Washington (District of Columbia); Remote; USD 261,000 - 330,000; Full time

Job summary

An innovative biotechnology company seeks a Clinical Research Medical Director to lead pivotal studies in obesity and related metabolic diseases. This role offers the opportunity to contribute to groundbreaking research while collaborating with diverse teams to integrate scientific and commercial insights. With a focus on patient care and professional growth, the position promises a competitive salary, comprehensive benefits, and the chance to make a significant impact in the field. Join a forward-thinking organization dedicated to serving patients and pushing the boundaries of medical science.

Benefits

Comprehensive benefits

Competitive salary

Bonuses

Stock incentives

Generous time-off

Flexible work arrangements

Qualifications

• 2+ years of clinical research experience required.
• Strong background in endocrinology preferred.

Responsibilities

• Lead clinical studies for AMG 133 in obesity and metabolic diseases.
• Collaborate with teams for evidence generation and regulatory input.

Skills

Clinical Research

Endocrinology

Communication Skills

Problem-Solving Skills

Education

MD or DO degree

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. Join us.

Clinical Research Medical Director, Endocrinology/Obesity - US Remote

What you will do

The Cardiovascular/Metabolic Therapeutic Area is seeking a Clinical Research Medical Director to lead one or more studies within the maridebart cafraglutide (AMG 133) global development program in obesity and related metabolic diseases. The position is based in Thousand Oaks, California, with potential for remote work. The role reports directly to the Global Development Lead for the AMG 133 program.

Responsibilities

1. Provide clinical/scientific expertise in the development, design, execution, and communication of the global evidence generation plan for the AMG 133 phase 3 program.
2. Support cross-functional and global collaborations to integrate medical, scientific, and commercial input into the development program.
3. Participate in safety and regulatory interactions, providing clinical input.
4. Interpret and communicate clinical trial data effectively.
5. Author clinical study reports, scientific publications, and regulatory submissions.
6. Develop relationships with key opinion leaders and present at advisory boards, scientific meetings, and external committees as delegated.
7. Contribute clinical content to Scientific Affairs and Commercial Organization materials.
8. Assist in developing Target Product Profiles (TPP) and Global Product Safety (GPS).
9. Create development options and present them to the Global Development Review Committee (GDRC) and Therapeutic Area Governance (TAG).
10. Collaborate with TA leadership and extended teams to develop development options.
11. Engage with specialized centers (CfDA, CfOR, CPMS) to explore innovative development strategies.

What we expect of you

We value diverse contributions to serve patients. The ideal candidate will have:

Basic Qualifications

• MD or DO degree from an accredited medical school
• At least 2 years of clinical research and/or basic science research experience

Preferred Qualifications

• Five or more years of experience in late clinical development within a pharmaceutical setting
• Experience in clinical research and/or basic science research combined with clinical teaching and patient care
• Strong background in endocrinology or related fields, with relevant subspecialty accreditation
• Knowledge of pharmaceutical development, product lifecycle, and commercialization
• Experience designing clinical studies in obesity or diabetes, including Phase 1-3 trials
• Understanding of GCP, FDA, EMEA/CHMP regulations, and international guidelines
• Leadership potential in a complex matrix environment
• Excellent communication skills, both written and oral
• Strong interpersonal and problem-solving skills with sound judgment

What you can expect from us

We support our team’s professional and personal growth, offering comprehensive benefits, competitive salary, bonuses, stock incentives, generous time-off, flexible work arrangements, and more.

The annual base salary range in the U.S. is $261,969 - $329,723, with actual compensation based on experience and qualifications.

We also offer a Total Rewards Plan including health benefits, retirement plans, bonuses, stock options, and flexible work models.

Join us

Apply now for a career that defies imagination. At Amgen, we aim to serve patients above all else. Join us.

careers.amgen.com

Application process

There is no set application deadline; we accept applications until the position is filled or a suitable candidate is found.

Amgen is an Equal Opportunity Employer and provides accommodations for individuals with disabilities upon request.