💼 About This Role

You'll manage and oversee ophthalmic clinical trial sites as a field-based monitor, ensuring compliance with ICH-GCP guidelines and regulatory requirements. You'll build strong relationships with investigators and site staff while conducting remote and on-site monitoring visits to ensure data quality and patient safety.

🎯 What You'll Do

• Manage clinical trial site activities to ensure compliance with protocols and regulations.
• Conduct remote and on-site monitoring visits including initiation and close-out.
• Review and verify source data for accuracy and completeness.
• Support site selection and qualification activities.

📋 Requirements

• Bachelor's degree with at least 3 years of experience as a Clinical Research Associate.
• Strong understanding of ICH-GCP guidelines and clinical trial regulations.
• Proven ability to conduct monitoring visits and assess site compliance.
• Experience verifying source data and ensuring consistency with trial records.

✨ Nice to Have

• Ophthalmology clinical research experience.
• Proficiency with CTMS and EDC systems.
• Experience in site qualification and selection.

🎁 Benefits & Perks

• 🏥 Comprehensive medical, dental, and vision insurance starting day one.
• 💼 401(k) with company match and competitive compensation.
• 🏖️ Flexible PTO and unlimited sick time plus 14 paid holidays.
• 👶 Paid parental leave up to 16 weeks with adoption assistance.
• 🏡 Remote work and wellness reimbursement program.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 1 hour
3. 3Technical assessment· 1 hour

🚩 Heads Up

• Travel up to 75% required