🛠 Tech Stack

💼 About This Role

You'll lead the LATAM PV system to ensure regulatory compliance for rare disease treatments. You'll drive safety data management and inspection readiness for a growing portfolio. This role offers the chance to make a meaningful impact in a collaborative global team.

🎯 What You'll Do

• Develop and maintain relationships with key stakeholders and vendors
• Support establishment and continuous improvement of LATAM PV system
• Contribute to submission of PV deliverables to regulatory authorities
• Support and perform quality review of ICSR follow-up activities

📋 Requirements

• Health care professional with degree in life sciences or allied health
• Minimum 5 years Pharmacovigilance experience
• Excellent oral and written communication skills in English and Spanish
• Regulatory databases knowledge including Veeva Vault and ARGUS

✨ Nice to Have

• Post-graduation in biotechnology
• Rare disease experience
• SmartSheet management experience

🎁 Benefits & Perks

• 🏖️ Generous vacation time and public holidays
• 📈 Long term incentive and Employee stock purchase plans
• 🧘 Employee wellbeing benefits
• 💪 Fitness reimbursement
• 🎓 Tuition sponsoring and professional development plans

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Panel interview· 60 min

🚩 Heads Up

• Role is contractor but requires 5+ years experience and senior level
• Mix of managerial and individual contributor responsibilities
• Requires both English and Spanish fluency without explicit compensation for language skills