💼 About This Role

You'll oversee clinical trial site management to ensure patient safety, data integrity, and regulatory compliance. You will conduct site visits and manage study start-up activities, building strong relationships with investigators. This field-based role offers exposure to complex therapeutic areas like oncology.

🎯 What You'll Do

• Oversee clinical trial site management for patient safety and data integrity
• Conduct qualification, initiation, monitoring, and close-out visits
• Manage study start-up activities and regulatory submissions
• Perform data review in EDC systems and resolve queries

📋 Requirements

• Bachelor's degree in scientific, healthcare, or related discipline
• 2+ years as a Clinical Research Associate in CRO, biotech, or pharma
• Strong understanding of GCP and ICH guidelines
• Willingness to travel up to 60%

✨ Nice to Have

• Experience in oncology trials
• Familiarity with EDC systems

🎁 Benefits & Perks

• 💰 Competitive salary $91,500 - $137,300
• 🏥 Health, dental, and vision insurance
• 🏖️ Paid time off including vacation and sick leave
• 👶 Paid parental leave and family support programs
• ✈️ Travel allowances and international collaboration opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Offer· N/A