🛠 Tech Stack

💼 About This Role

You'll lead pharmacovigilance activities for clinical programs in a fast-growing biotech environment. Your work will directly support patient safety and regulatory compliance for innovative therapies targeting severe autoimmune diseases. This remote role offers high-impact exposure across safety governance and cross-functional collaboration.

🎯 What You'll Do

• Oversee pharmacovigilance activities for assigned clinical programs
• Review and assess adverse event reports for accuracy and regulatory reporting
• Lead DSMB and Safety Review Committee meetings, including materials preparation
• Contribute to aggregate safety reporting like DSUR submissions

📋 Requirements

• PharmD or Registered Nurse (RN) degree required
• Experience in pharmacovigilance or clinical development in pharma/biotech
• Proven experience reviewing adverse events and working with safety physicians
• Hands-on experience supporting DSMB and SRC processes

✨ Nice to Have

• Experience in rare disease or oncology programs
• Prior experience in early-stage biotech or high-growth environments

🎁 Benefits & Perks

• 💰 Competitive compensation aligned with experience and industry standards
• 🏠 Remote work flexibility within the United States
• 🧠 Professional growth opportunities in pharmacovigilance leadership
• 💡 Exposure to high-impact clinical development programs
• 🤝 Collaborative, mission-driven culture focused on patient outcomes

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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