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انتهت بتاريخ ١ أبريل ٢٠٢٦
وصف الوظيفة
As part of our global team, you’ll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. You will conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
المسؤوليات
- Monitor investigator sites with a risk-based monitoring approach
- Ensure data accuracy through SDR, SDV and CRF review
- Assess investigational product through inventory and records review
- Document observations in reports and letters
- Initiate clinical trial sites ensuring compliance with protocol
- Facilitate communication between investigative sites and project teams
المؤهلات
- Bachelor's degree in a life sciences related field or Registered Nursing certification
- Minimal clinical monitoring experience (comparable to 2 years)
- Valid driver's license
- Basic medical/therapeutic area knowledge
- Good organizational and time management skills
- Ability to travel 60-80%