Hybrid Drug Safety & Benefit-Risk Scientist

UCB; Atlanta (GA); Hybrid; USD 126,000 - 165,000; Full time

Job summary

UCB is seeking a Drug Safety & Benefit‑Risk Scientist to join our Patient Safety team at the US Headquarters near Atlanta, GA. The role focuses on evaluating safety and benefit‑risk data across development and post‑marketing steps, informing regulatory submissions, and maintaining inspection‑ready documentation.

With 1+ years in drug safety or pharmacovigilance and strong scientific writing, you may lead complex assessments and mentor colleagues while collaborating with global teams.

Qualifications

• Master's, PhD, or PharmD in a relevant discipline.
• 1+ years of experience in drug safety or pharmacovigilance.
• 1+ years of experience interpreting complex clinical, safety and scientific data.
• Strong scientific writing and safety documentation skills.

Responsibilities

• Evaluate safety and benefit‑risk data for development and marketed products.
• Prepare safety assessments and benefit‑risk documentation for regulatory submissions.
• Interpret clinical and safety data for cross‑functional decision‑making.
• Support signal evaluation, risk management and safety monitoring strategies.
• Maintain inspection‑ready documentation and strengthen safety processes.
• Lead complex assessments and mentor colleagues, depending on experience.

Skills

Drug safety

Pharmacovigilance

Scientific writing

Data interpretation

Mentoring

Education

Master's/PhD/PharmD

Job description

UCB is seeking a Drug Safety & Benefit‑Risk Scientist to join our Patient Safety team at the US Headquarters near Atlanta, GA. The role focuses on evaluating safety and benefit‑risk data across development and post‑marketing steps, informing regulatory submissions, and maintaining inspection‑ready documentation.

With 1+ years in drug safety or pharmacovigilance and strong scientific writing, you may lead complex assessments and mentor colleagues while collaborating with global teams.