Clinical Research Associate- Wound Care Experience Required

📋 Description

• Independently conduct qualification, initiation, interim, and close-out visits, both remotely and
• Prepare accurate, timely monitoring reports detailing site issues, resolutions, actions taken
• Review source documentation and verify case report form (CRF) data for accuracy, completeness, and
• Ensure adherence to ICH GCP guidelines, applicable FDA regulations, local regulatory requirements
• Maintain regular communication with investigators and site teams, respond to sponsor requests
• Facilitate adverse event reporting, reconcile serious adverse event (SAE) reports with source

🎯 Requirements

• Bachelor's degree in Biology, Life Sciences, or a related scientific field.
• At least 2 years of experience monitoring wound care clinical trials.
• Strong understanding of clinical research practices, ICH GCP, applicable local regulations, and
• Proven ability to autonomously manage clinical trial monitoring activities, prioritize
• Good computer skills, including experience with clinical trial management systems, clinical trial
• Excellent communication and interpersonal skills, with the ability to build positive, productive

🎁 Benefits

• Competitive salary: The original posting lists a salary range of $95,000–$120,000. The final offer
• Remote work options: The position is advertised as remote, with opportunities listed across the
• Professional development: Opportunities to develop clinical research expertise and grow
• Flexible work programs: Flexible work arrangements are highlighted as part of the broader employee
• Global collaboration and travel: Opportunities to work with international colleagues and engage
• Collaborative work environment: Join a multidisciplinary, international team that values