Added
2 days ago
Location
Type
Full time
Salary
Salary not provided

Related skills

ms office gcp edc ms project etmf

📋 Description

  • Manage clinical elements of trials across multiple countries.
  • Lead CRAs and coordinate site start-up, enrollment, monitoring, and close-out.
  • Ensure regulatory documentation and cross-functional oversight of trials.
  • Mentor and train team members.
  • Identify risks to timelines and develop action plans with sponsors.
  • Maintain cross-functional partnerships to deliver client satisfaction.

🎯 Requirements

  • Bachelor’s degree or equivalent in science/health (oncology preferred)
  • Experience leading clinical studies across multiple countries in CRO/Pharma
  • Significant oncology clinical trial management experience
  • Strong knowledge of GCP/ICH guidelines and clinical development
  • Willingness to travel domestically and internationally
  • Excellent English communication skills
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