🛠 Tech Stack

💼 About This Role

You'll monitor ophthalmic clinical trials, ensuring ICH-GCP compliance across study sites. You'll build relationships with investigators while verifying data integrity and patient safety. This remote role offers direct exposure to all phases of clinical trial execution.

🎯 What You'll Do

• Conduct remote/on-site monitoring visits for regulatory compliance
• Develop and maintain strong relationships with clinical sites
• Review clinical data for accuracy and GCP adherence
• Manage essential regulatory documentation in CTMS/eTMF

📋 Requirements

• Bachelor's degree with at least 2 years CRA experience
• ICH-GCP guidelines and clinical trial regulations knowledge
• Site monitoring experience including source data verification
• CTMS and EDC system proficiency

✨ Nice to Have

• Ophthalmology clinical research experience
• Multilingual abilities

🎁 Benefits & Perks

• 🏥 Medical, dental, vision insurance from day one
• 🏖️ Flexible PTO with unlimited sick time
• 💰 401(k) matching retirement plan
• 👶 Paid parental leave and fertility support
• 💻 Remote work support and wellness reimbursement

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical Panel· 60 min