Clinical Research Associate

• Initiate, monitor, and close out study sites during study conduct
• Monitor clinical trials on-site and remotely according to SOPs, GCP, ICH guidelines, sponsor requirements, and applicable regulations
• Perform monitoring activities to ensure subject safety, data integrity, and quality
• Verify informed consent procedures and protocol compliance
• Review electronic or paper CRFs and subject source documentation for validity, completeness, and accuracy
• Verify management and accountability of Investigational Product
• Prepare monitoring visit reports, document findings and follow-up actions, update tracking systems, and escalate issues
• Maintain site documentation and support eTMF and ISF compliance
• Update CTMS and other project systems with accurate site information

• Bachelor's Degree, preferably in Life Sciences, Nursing, or equivalent
• Minimum 1 year of relevant clinical research experience or relevant academic background related to clinical trials or clinical development activities
• Understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements
• Strong written and verbal communication skills with fluency in English
• Excellent organizational skills
• Ability to work independently and within a matrix team environment

• Competitive compensation package
• Comprehensive benefits
• Opportunity for personal and professional growth
• Collaborative and innovative work environment