🛠 Tech Stack

💼 About This Role

You'll support clinical trial operations for a cancer detection company, maintaining trial master files and tracking site payments and vendor invoices. Your work helps bring innovative screening technologies to patients.

🎯 What You'll Do

• Maintain and review Trial Master File (TMF) for completeness and accuracy
• Track site payments and vendor invoices
• Assist in tracking and reporting key study quality metrics
• Support development of tracking tools and internal processes

📋 Requirements

• Bachelor’s degree in a related scientific discipline
• 1 year of relevant pharmaceutical/biotech/medical device experience
• Working knowledge of GCPs and Trial Master Files
• Experience with eTMF system and strong database skills

✨ Nice to Have

• Positive self-starter with ability to adapt to changing priorities
• Ability to establish and maintain effective working relationships in a team environment

🎁 Benefits & Perks

• 🏖️ Paid Time Off
• 🏥 Health Insurance
• 📈 401(k) Matching

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Phone Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Team Interview· 60 min