🛠 Tech Stack

💼 About This Role

You'll develop strong site relationships and ensure compliance with ICH/GCP and regulations across all trial phases. Your core impact is managing clinical study sites and ensuring data accuracy for ophthalmic drug development. This role offers the chance to work with a leading ophthalmic CRO.

🎯 What You'll Do

• Perform remote and on-site monitoring visits and document findings
• Review regulatory documentation for study start-up and maintenance
• Communicate with investigators on protocol conduct and deviations
• Manage information in CTMS, eTMF, and other systems

📋 Requirements

• Bachelor's degree with 2 years' experience as a Clinical Research Associate
• Knowledge of ICH/GCP and federal regulations
• Proficiency with Excel, CTMS, and EDC
• Ability to conduct site visits including initiation and close-out

✨ Nice to Have

• Ophthalmic experience
• Multilingual communication

🎁 Benefits & Perks

• 💷 Structured pension plan
• 🏥 Private medical insurance (Vitality and SimplyHealth)
• 🛡️ Company paid life and disability insurance

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Interview with Hiring Manager· 45 min
3. 3Technical/Behavioral Interview· 60 min
4. 4Offer· N/A