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Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com Ā  and follow us on www.twitter.com/amgen

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šŸ¢ Amgen
šŸ’° $28.5B Post-IPO Debt on 2022-12-12šŸ«‚ on 2023-10-24Biotechnology Research
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šŸ”„ Clinical Research Medical Director - Cardiology/Heart Failure, US - Remote
Posted 2024-10-21

šŸ“ United States

šŸ§­ Full-Time

šŸ’ø 256334 - 318868 USD per year

šŸ” Biotechnology

  • MD or DO degree from an accredited medical school.
  • Minimum of 2 years of clinical research experience and/or basic science research.
  • Preferred 5 years of experience in late clinical development within a pharmaceutical organization.
  • Strong clinical development experience in cardiology or relevant sub-specialty.
  • Knowledge of pharmaceutical product development and commercialization processes.
  • Experience developing clinical study concepts and trial designs.
  • Knowledge of Good Clinical Practices (GCP), FDA, and relevant international regulations.
  • Leadership experience in a complex matrix environment.
  • Ability to present complex medical concepts effectively.

  • Provide clinical/scientific knowledge into the development and execution of the global evidence generation plan for the AMG 133 phase 3 program.
  • Support cross-functional and global collaborations to integrate medical, scientific, and commercial input.
  • Participate in safety and regulatory interactions and provide clinical trial data interpretation.
  • Author clinical study reports and regulatory submissions.
  • Develop key opinion leaders and present at advisory boards.
  • Provide clinical content input to scientific and commercial materials.
  • Contribute to TPP and Global Product Safety development.
  • Create development options for the Global Dev Review Committee.

LeadershipCross-functional Team LeadershipCommunication SkillsCollaborationProblem Solving

Posted 2024-10-21
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