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

Related skills

ms office edc ms project etmf ctms

📋 Description

  • Manage clinical elements across trials in multiple countries
  • Lead CRAs and oversee site monitoring and regulatory activities
  • Ensure trial timelines, quality, and deliverables are met
  • Oversee site start-up, enrolment, data cleaning, and close-out
  • Mentor and train team members; communicate clearly
  • Identify risks and develop proactive mitigation plans

🎯 Requirements

  • Experience leading multi-country trials in CRO/Pharma/Biotech
  • Significant oncology trial management experience
  • GCP/ICH guidelines knowledge and development process
  • Domestic and international travel availability
  • Fluent English communication
  • Bachelor’s degree in science/health field

🎁 Benefits

  • Remote work options across Europe
  • Work on oncology-focused clinical trials
  • Collaborative, growth-oriented culture
  • Equal Opportunity Employer
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