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Role Overview:
- Monitor wound care clinical trials independently, ensuring data integrity and GCP compliance.
Key Responsibilities:
- Conduct site qualification, initiation, interim, and close-out visits.
- Prepare monitoring reports and verify CRF data for accuracy.
- Facilitate safety reporting and investigational product accountability.
What We Offer:
- Remote work options and flexible work programs.
- Professional development and global collaboration opportunities.
- Purpose-driven work in clinical research with a collaborative culture.
Partner Company
The company is a clinical research organization focused on wound care trials. It offers a collaborative, international, and innovation-driven culture with opportunities for professional development and flexible remote work.