Medical Sciences Director

3 days ago

Washington, Washington, D.C., United States Amgen Full time

Job Summary

We are seeking a highly skilled Medical Sciences Director to join our Oncology Late Development Group. As a key member of our team, you will contribute to the late phase clinical development of oncology, collaborating with cross-functional teams to define, design, and deliver late phase clinical results.

Key Responsibilities

  • Provide subject matter expertise in clinical and translational trial science, as well as the biology and treatment of cancer.
  • Contribute intellectual insight into experimental design and data analysis.
  • Serve as an internal clinical expert in translational and clinical oncology.
  • Support medical monitor in clinical trials and assist in resolving issues that may arise.
  • Provide guidance and assistance in the identification and management of oncology collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects.

Requirements

  • Doctorate degree and 4 years of life sciences/healthcare experience.
  • Master's degree and 7 years of life sciences/healthcare experience.
  • Bachelor's degree and 9 years of life sciences/healthcare experience.
  • 5 years of pharmaceutical clinical drug development experience.
  • Strong preference for individuals with proven track record of thoracic oncology clinical trial process improvement.
  • Industry or academic experience in late-phase oncology drug development.
  • Strong communication & presentation skills to clearly communicate scientific concepts /data to leadership committees both internally or externally (both written and oral).
  • Experience with designing, monitoring, and implementing oncology clinical trials and interpreting test results in compliance with Good Clinical Practice standards and regulatory requirements.
  • Understanding of conducting study data readout activities, including data cleaning, data base lock, data extract, producing outputs of data.
  • Experience drafting high level submission documents for regulatory submissions including authoring clinical regulatory responses for health regulatory interactions.
  • Serving as a contributing author to scientific publications and data presentations at scientific conferences.
  • Experience in clinical data analysis such as Spotfire or other data analysis tools.

About Amgen

Amgen is an Equal Opportunity employer and will consider you without regard to your 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.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities.

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