Global Development Medical Director — Late-Stage Trials

ASTRAZENECA UK LIMITED

Cambridge

Hybrid

GBP 120,000 - 180,000

Full time

2 days ago
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Job summary

AstraZeneca UK Limited is seeking a Global Development Medical Director to lead medical and scientific activities across late-stage respiratory and immunology programs. You will design and interpret pivotal trials, build networks with external experts, and work with Safety, Regulatory, Clinical Operations, and other functions in a truly international setting.

The role emphasizes leadership in trial design and regulatory inputs, with responsibility for medical monitoring, publications, and

Qualifications

  • MD/PhD or MD required.
  • 3+ years in pharmaceutical industry and 3+ years in clinical research.
  • Demonstrated partnership and collaboration across countries and cultures.
  • Fluent in oral and written English with strong presentation skills.
  • Background in pulmonary medicine, immunology, rheumatology, allergy or dermatology preferred.

Responsibilities

  • Provide medical and scientific leadership in late-stage development of respiratory and immunology medicines.
  • Lead design, execution and interpretation of pivotal clinical trials.
  • Build relationships with external scientific experts.
  • Collaborate with Patient Safety, Regulatory Affairs and Clinical Operations.
  • Lead medical monitoring of trials.
  • Prepare regulatory documents and interact with regulatory authorities.
  • Develop and review protocols, informed consent, and investigator's brochure.
  • Participate in preparation of scientific publications and conference presentations.
  • Maintain fluent English and clear cross-country communication.
  • Ideal candidate has background in pulmonary medicine, immunology, rheumatology, allergy, or dermatology.

Skills

Fluent English
Leadership & collaboration
Presentation skills

Education

MD or MD/PhD Degree

Job description

AstraZeneca UK Limited is seeking a Global Development Medical Director to lead medical and scientific activities across late-stage respiratory and immunology programs. You will design and interpret pivotal trials, build networks with external experts, and work with Safety, Regulatory, Clinical Operations, and other functions in a truly international setting.

The role emphasizes leadership in trial design and regulatory inputs, with responsibility for medical monitoring, publications, and

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