Make your mark for patients
We are seeking to hire an exceptional Drug Safety & Benefit-Risk Scientist who is analytical collaborative and adaptable to join our Patient Safety team. This position will be based out of our US Headquarters near Atlanta GA.
About the role
You will evaluate medicine safety and benefit-risk profiles across clinical development and post-approval activities. Your scientific assessments will inform evidence-based decisions regulatory submissions and safety strategies throughout the medicine lifecycle. You will interpret complex data communicate clear conclusions and help maintain high-quality inspection-ready documentation. Depending on experience you may also lead complex assessments mentor colleagues and provide scientific guidance across projects.
Who youll work with
You will be working in a team that partners closely with medical clinical development regulatory epidemiology and safety experts. Together you will integrate evidence from multiple sources support informed benefit-risk decisions and strengthen safety monitoring across the medicine lifecycle. You will collaborate with global multidisciplinary stakeholders while contributing to consistent scientific standards and continuous process improvement.
What youll do
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.
Interested For this role were looking for the following:
Minimum requirements
Masters 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.
Preferred requirements
Experience supporting benefit-risk assessments during clinical development.
Knowledge of global pharmacovigilance regulations and safety practices.
Experience preparing regulatory safety documentation.
Experience supporting signal detection and risk management activities.
Demonstrated project leadership or colleague mentoring experience.
Experience collaborating across global multidisciplinary teams.
Salary
This positions reasonably anticipated base salary range is $125600 to $164900 per year. The actual salary offered will consider internal equity and may also vary depending on the candidates region job-related knowledge skills and experience among other factors.
Are you ready to go beyond to create value and make your mark for patients If this sounds like you then we would love to hear from you!
About us
UCB is a global biopharmaceutical company focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe inspired by patients and driven by science.
Why work with us
At UCB we dont just complete tasks we create value. We arent afraid to push forward collaborate and innovate to make our mark for patients. We have a caring supportive culture where everyone feels included respected and has equal opportunities to do their best work. We go beyond to create value for our patients and always with a human focus whether thats on our patients our employees or our planet. Working for us you will discover a place where you can grow and have the freedom to carve your own career path to achieve your full potential.
At UCB weve embraced a hybrid-first approach to work bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employment decisions will be made without regard to any characteristic protected by applicable federal state or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment your employment with UCB or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws orders and regulations.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.Required Experience:
IC
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