Clinical Research Associate- Wound Care

📋 Description

• Conduct site qualification, initiation, interim, and close-out visits remotely and onsite, ensuring
• Prepare accurate and timely monitoring visit reports covering site issues, resolutions, corrective
• Review source documents and verify case report form (CRF) data to ensure accuracy, completeness
• Ensure compliance with ICH GCP guidelines, applicable FDA requirements, local regulations, ethical
• Maintain regular communication with investigators and site staff, respond to questions, monitor
• Facilitate adverse event reporting, reconcile serious adverse event (SAE) reports, and ensure

🎯 Requirements

• Bachelor's degree in Biology, Life Sciences, or a related scientific discipline
• At least 2 years of experience monitoring wound care clinical trials (required)
• Strong knowledge of clinical research practices, ICH GCP, local regulatory requirements, and
• Demonstrated ability to manage clinical trial monitoring activities autonomously, prioritize tasks
• Good computer skills and experience using clinical trial management systems, clinical trial
• Excellent written and verbal communication skills, with the ability to establish and maintain

🎁 Benefits

• Remote work options (locations across the Americas; availability for Brazil to be confirmed)
• Competitive salary range of $90,000–$130,000 (final offer depends on location, experience, and
• Professional development opportunities
• Flexible work programs
• Global collaboration and travel opportunities
• Creative and collaborative culture