Clinical Research Associate II: Lead Trials and Data Management

Take the lead as a Clinical Research Associate II and influence clinical trial success. Focus on data quality, compliance, and cross-functional collaboration to innovate patient treatments. This position emphasizes your strategic involvement in clinical study processes. With a minimum of 2 years' experience, you will conduct essential site activities from qualification to close-out. Your background in scientific research and effective communication will benefit the team and trial integrity. Key Responsibilities:

• Execute site qualification, monitoring, and close-out activities
• Ensure adherence to the clinical trial protocol
• Resolve data queries and maintain high standards
• Collaborate with site investigators and staff
• Prepare and review essential study documentation Requirements:
• Bachelor's degree in a relevant scientific field
• Minimum of 2 years in clinical research roles
• Understanding of clinical trial guidelines
• Strong organizational and detail-oriented skills
• Flexibility to travel 60% of the time Leverage your clinical expertise to enhance study procedures and contribute meaningfully to health innovations.