Clinical Research Associate II - FSP

📋 Description

• Oversees site management to protect patient safety and data quality.
• Guides audit readiness and follow-up actions.
• Maintains trial tools, tracking systems, and status reports.
• Manage site start-up tasks and regulatory submissions.
• Perform on-site and remote monitoring per protocol.
• Document activities and support recruitment and retention.

🎯 Requirements

• 4-year degree in a scientific or healthcare field.
• 2+ years as a CRA in CRO/pharma or biotech.
• Excellent communication and organizational skills.
• Experience monitoring oncology trials.
• Proficient with electronic systems, spreadsheets, and email.
• Ability to travel up to 60% and internationally.

🎁 Benefits

• Discretionary annual bonus.
• Health insurance.
• Retirement savings benefits.
• Life and disability insurance.
• Parental leave.
• Paid time off for sick leave and vacation.