This role focuses on early development (phase I) and late stage (phase II-III) safety science activities for a global biotechnology company fighting cancer
Job Summary
This role focuses on early development (phase I) and late stage (phase II-III) safety science activities for a global biotechnology company fighting cancer.
The position requires leading signal evaluation, safety monitoring, and the preparation of critical regulatory documents such as DSURs and Package Inserts.
BeOne offers competitive compensation including base salary, annual bonus eligibility, discretionary equity awards, and a comprehensive benefits package.
Matching Summary
This role focuses on early development (phase I) and late stage (phase II-III) safety science activities for a global biotechnology company fighting cancer.
Salary
Base: $154,300.00 - $204,300.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off
Skills & Requirements
Must-have
Signal detection and assessment
Safety data analysis
Regulatory submission authoring
Pharmacovigilance expertise
ICH standards compliance
Nice-to-have
Collaborative team spirit
Patient-first mindset
Bold ingenuity
Cross-functional leadership
Continuous learning attitude
Key Requirements
PharmD or PhD in medical/biological field
4+ years pharmacovigilance analytical experience
MD with residency or equivalent clinical training
2+ years pharmaceutical industry safety experience