Senior Clinical Research Associate

Corcept is seeking a Senior Clinical Research Associate to manage clinical aspects of studies, work with cross-functional teams, and ensure compliance with protocol and good clinical practices. The role requires on-site presence and may involve travel.

Requirements

• Manage all clinical aspects of a small to medium-sized clinical study or assume significant management responsibilities on a large-scale study
• Work closely with cross-functional teams, vendors, sites, and CRO (when applicable)
• Implement and monitor clinical study activities to assure adherence to good clinical practices (GCPs), standard operating procedures (SOPs), and study protocols
• Support the Study Lead in clinical study activities
• Participate in protocol development and tracking changes for future protocol amendments
• Oversee aspects of study management and vendors to ensure high quality of data
• Review and negotiate site budgets and contracts
• Conduct sponsor oversight visits and site qualification visits and site initiation visits
• Maintain a complete and updated regulatory file for each assigned site

Benefits

• Health insurance
• Paid time off
• Retirement plan
• Life insurance
• Disability insurance
• Dental insurance
• Vision insurance
• Flexible spending account
• Stock options