Senior Clinical Research Associate, Field Monitor

Responsibilities

• Develop and update training materials and study documentation
• Interpret study protocols, logistics, risks, and data evaluation methods
• Serve as a Subject Matter Expert guiding clinical sites on protocols and eligibility
• Create and manage site feasibility questionnaires and essential document collection
• Oversee data review and resolve issues in collaboration with Clinical Research Associates

Qualifications

• Bachelor's degree in clinical research, science, or health-related field with 6 years of experience, or a high school diploma with 8 years of experience in clinical research
• Minimum of 2 years as a Clinical Research Associate II or higher is required
• Proficiency in MS Office Suite and familiarity with EDC, eTMF, CTMS systems
• Strong communication skills, both written and oral, across diverse stakeholders
• Ability to work independently and manage multiple priorities

Benefits

• Comprehensive Medical, Dental, and Vision plan options
• Health and Financial Wellness Programs; Employee Assistance Program
• 401(k) Retirement Plan with Company Match
• Flexible Spending Accounts for healthcare and dependent care
• Unlimited PTO for exempt employees and generous vacation policies