🛠 Tech Stack

💼 About This Role

You'll support day-to-day operations of a Phase 3 clinical trial, including trial conduct and close-out activities. You'll coordinate tracking, regulatory documents, and vendor activities to ensure study progress. This role offers remote work and the chance to contribute to groundbreaking gene therapies.

🎯 What You'll Do

• Coordinate tracking of clinical trial documents and TMF filing
• Maintain tracking spreadsheets for study progress and essential documents
• Track and coordinate CRO and third-party vendor activities
• Assist in creation and maintenance of study materials and training documents

📋 Requirements

• Bachelor's degree
• At least 5 years of clinical trial support experience
• Basic knowledge of ICH GCP Guidelines and regulatory requirements
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, SharePoint, Outlook)

✨ Nice to Have

• Experience with EDC/CTMS systems
• Experience with Phase 3 trials
• Familiarity with TMF/eTMF

🎁 Benefits & Perks

• 💰 Competitive base salary with annual bonus potential
• 🏖️ Remote work flexibility
• 🏥 Comprehensive benefits package (medical, dental, vision)
• 📈 Career development opportunities in a late-stage biotech
• 🏢 Collaborative team environment

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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

🚩 Heads Up

• Temporary role with unclear duration
• Requires 5+ years experience but titled 'Associate'