Clinical Research Associate, Sponsor Dedicated

Requirements

• Perform site monitoring visits
• Work with sites to adapt 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 site documents are available for filing
• Create and maintain documentation regarding site management
• Collaborate with study team members

Benefits

• Bonus
• Health and welfare benefits