Senior Clinical Research Associate

Position Summary:

• Handles complex assignments with wide-ranging experience.
• Manages clinical trials and supports Clinical Trial Managers.
• Focuses on training and mentoring junior staff.

Responsibilities:

• Protects patient safety and data quality at managed sites.
• Manages study-specific tools, systems, and reports.
• Manages site start-up procedures and investigator contracts.

Site Visits & Monitoring:

• Independently conducts all forms of site visits.
• Prepares accurate and timely monitoring reports.
• Documents activities and supports patient recruitment.

Additional Tasks:

• Performs data review and assists with data discrepancies.
• Identifies site risks and escalates them to the Clinical Trial Manager.
• Prepares for and attends Investigator Meetings.