🛠 Tech Stack

💼 About This Role

You'll act as a customer advocate, overseeing clinical study sites and ensuring compliance with GCP and regulatory requirements. Your work will directly impact the integrity of clinical data and the safety of study patients. This role offers the chance to mentor junior CRAs and work with a collaborative team.

🎯 What You'll Do

• Conduct routine monitoring and close-out of clinical sites
• Organize and maintain clinical study documentation for audits
• Provide sponsor oversight of monitoring activities delegated to CRO
• Assist in development of study-specific monitoring procedures

📋 Requirements

• Bachelor's degree in life science or related health profession
• Minimum 5 years clinical research monitoring experience
• Pharmaceutical and ophthalmology experience required
• Thorough knowledge of ICH/GCP R3 Guidelines

✨ Nice to Have

• Vendor oversight experience
• Mentoring experience

🎁 Benefits & Perks

• 🏖️ Generous paid time off including vacation, holidays, personal days
• 🏥 Health, dental, and vision insurance
• 💰 Bonus and stock equity
• 🏢 Onsite gym, pool, snacks, drinks, catered meals

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical/skills interview· 60 min
4. 4On-site panel interview· half day