Related skills
pharmacovigilance vendor_oversight📋 Description
- Lead pharmacovigilance activities for investigational products.
- Direct drug safety oversight for select clinical trials and case processing.
- Oversee CRO safety operations, case processing, and data exchange.
- Lead safety sections of regulatory submissions and safety docs.
- Participate in regulatory authority meetings and advisory panels.
- Develop proactive risk management for investigational compounds.
🎯 Requirements
- Post-graduate degree (MD/DO) or international equivalent.
- Excellent communication and interpersonal skills.
- 12+ years in industry; at least 9 years senior drug safety.
- Experience in both clinical development and post-marketing safety.
- Regulatory submission experience.
- 1–3 years of project leadership/management experience.
🎁 Benefits
- Market-leading compensation
- 401(k) with employer match
- Comprehensive health benefits
- 100% employer-paid medical, dental and vision for you and dependents
- Hybrid work model with flexibility
- Subsidized lunch and parking
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