Clinical Research Associate, Sponsor Dedicated

Requirements

• Perform site monitoring visits
• Work with sites to adapt, drive, and track subject recruitment plan
• Administer protocol and related study training
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies
• Ensure copies/originals site documents are available
• Create and maintain appropriate documentation regarding site management

Benefits

• Health and welfare benefits
• Incentive plans
• Bonuses