Global Medical Director, Medical Affairs (Remote)

Worldwide Clinical Trials

Phoenix (AZ)

Remote

USD 135,000 - 268,000

Full time

8 days ago

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Job summary

Worldwide Clinical Trials is seeking a Medical Director, Medical Affairs to provide medical oversight across assigned studies and act as Medical Monitor for clinical trials. You will collaborate with cross-functional teams, contribute to protocol development and safety review, and interact with sponsors to drive successful outcomes.

This remote US role requires an MD, 2+ years of monitoring experience, and strong knowledge of GCP, safety processes, and regulatory requirements.

Qualifications

  • Medical degree required and at least 2 years of medical monitoring experience.
  • Strong knowledge of GCP, clinical development, safety processes and regulations.
  • Experience reviewing safety data and supporting SAE assessment and management.
  • Excellent written and verbal communication, presentation, organizational, and time management skills.
  • Proficiency with MS Word, Excel, and Access.

Responsibilities

  • Provide medical oversight and serve as the assigned Medical Monitor for clinical research studies.
  • Lead global and pan-regional trials as a Global Lead Medical Monitor, ensuring consistent medical guidance across study teams.
  • Review and support the medical management of serious adverse events in collaboration with Medical & Safety teams.
  • Deliver protocol-specific and therapeutic area training to project teams to support high-quality study execution.
  • Contribute clinical and scientific expertise to study protocols and clinical development programs.

Skills

Medical monitoring
GCP knowledge
Communication skills
Time management
English proficiency

Education

Medical degree

Tools

Microsoft Word
Microsoft Excel
Microsoft Access

Job description

Worldwide Clinical Trials is seeking a Medical Director, Medical Affairs to provide medical oversight across assigned studies and act as Medical Monitor for clinical trials. You will collaborate with cross-functional teams, contribute to protocol development and safety review, and interact with sponsors to drive successful outcomes.

This remote US role requires an MD, 2+ years of monitoring experience, and strong knowledge of GCP, safety processes, and regulatory requirements.

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