💼 About This Role

You'll lead cross-functional clinical trial activities, ensuring on-time, on-budget delivery in a collaborative biotech environment. Your core impact will be driving study startup and site management while overseeing CROs and vendors to maintain regulatory compliance. This role stands out for its direct involvement in oncology trials with radiopharmaceuticals.

🎯 What You'll Do

• Lead cross-functional study team meetings and coordinate activities.
• Drive study startup including feasibility, site selection, and timelines.
• Oversee CROs and vendors to ensure data integrity and compliance.
• Manage US clinical sites and perform monitoring visits as needed.

📋 Requirements

• 5-8 years of clinical operations experience in biotech or pharma.
• Extensive experience managing US clinical sites and start-up activities.
• Oncology experience preferably in solid tumors.
• Strong knowledge of GCP, ICH, and FDA regulations.

✨ Nice to Have

• Experience with radiopharmaceuticals.
• Experience in clinical data review and data management processes.
• Advanced degree in Life Sciences, Nursing, or Pharmacy.

🎁 Benefits & Perks

• 🏥 Health Insurance
• 💰 Competitive Salary
• 📈 Stock Options
• 🏖️ Paid Time Off
• 🏢 Onsite Work

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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