Medical Director, Early Cardiometabolic Clinical Development

BioSpace

Washington (District of Columbia)

Sur place

USD 180 000 - 280 000

Plein temps

Il y a 4 jours
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Avantages offerts par ce poste

Comprehensive employee benefits
Stock-based long-term incentives
Flexible work models

Résumé du poste

Amgen in the United States is seeking a Clinical Development Director to lead early phase programs in cardiometabolic/general medicine. You will drive protocol design, study startup, and cross-functional execution across internal teams and external partners.

You will review safety and pharmacokinetic data, guide biomarker strategies, and contribute to licensing discussions while shaping development plans and timelines for high-impact medicines.

Qualifications

  • MD or DO degree from an accredited medical school.
  • 2 years of industry or academic/basic sciences/clinical research experience.
  • Board certification or eligible; residency in cardiology or internal medicine.

Responsabilités

  • Lead early phase clinical development of cardiometabolic/general medicine candidates.
  • Support protocol development, study start-up, data review, monitoring and analysis.
  • Review safety, efficacy, pharmacodynamic and pharmacokinetic data.
  • Collaborate with internal teams and external experts to guide drug development.
  • Evaluate external licensing or partnering opportunities.
  • Contribute to external partnerships and strategic biomedical guidance.

Connaissances

Leadership
Interpersonal skills
Communication
Collaboration

Formation

MD or DO degree
Residency training in Cardiology/Internal Medicine
Board certification or eligible

Description du poste

Amgen in the United States is seeking a Clinical Development Director to lead early phase programs in cardiometabolic/general medicine. You will drive protocol design, study startup, and cross-functional execution across internal teams and external partners.

You will review safety and pharmacokinetic data, guide biomarker strategies, and contribute to licensing discussions while shaping development plans and timelines for high-impact medicines.

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