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Medical Director, Neuroimmunology, Global Patient Safety

AbbVie · North Chicago, IL · Full time · Research

Posted Oct 1, 2026 · We last checked this listing on Oct 6, 2026

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Likely interview questions for this role

Written from this job description, not a generic list. Each one notes what the interviewer is really checking.

About your past

Tell me about a time your clinical experience changed how you read safety data.

What they are checking: Whether they bring real patient care experience into reading safety data, which helps distinguish meaningful signals from noise.

Tell me about a time you disagreed with a colleague about whether something was a signal.

What they are checking: Whether they can debate signals scientifically and reach a sound conclusion, while keeping working relationships respectful and productive.

What would you do

A regulator asks a pointed question about a safety finding. How would you approach the response?

What they are checking: Whether they respond to regulators with careful judgment and clear evidence, since a poor response can affect a product's future.

How do you explain an aggregate safety analysis to a cross-functional team that isn't medical?

What they are checking: Whether they can explain aggregate safety analysis plainly to non-medical colleagues, so teams make informed decisions together.

About the work

Walk me through how you'd evaluate a potential safety signal for a neuroscience product.

What they are checking: Whether they evaluate safety signals in a structured way, including causality and aggregate data, which protects patients and supports regulatory decisions.

How would non-clinical toxicology findings shape your safety surveillance plan?

What they are checking: Whether they can apply toxicology findings to surveillance planning, since nonclinical results often predict what to watch for in patients.

What goes into a strong medical safety assessment?

What they are checking: Whether they write clear, well-reasoned safety assessments, because these documents drive decisions with regulators and internal leadership.

How does safety surveillance differ in clinical trials versus post-marketing?

What they are checking: Understanding of data sources and reporting rules in each setting.

What's in a risk management plan, and how do you keep it current?

What they are checking: Whether they understand risk management plans and keep them current, since outdated plans can leave real risks unaddressed.

How would you use epidemiology data to put a safety finding in context?

What they are checking: Whether they use background rates and epidemiology to put findings in context, avoiding both false alarms and missed signals.

Practice this interview out loud.

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The full job description

As published by AbbVie.

Purpose: Responsible for supporting the Product Safety Lead (PST) in overseeing the comprehensive safety surveillance of one or more neuroscience products throughout their lifecycle, including signal management, interpretation of pharmacovigilance regulations, and supporting all safety deliverables. Responsibilities: • Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance • Safety surveillance for pharmaceutical / biological / drug –device combination neuroscience products • Contribute to the authorship of key pharmacovigilance documents, including but not limited to medical safety assessments, periodic safety reports, regulatory responses and risk management plans • Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV documents • Analyze and interpret aggregate safety data and communicate these analysis and interpretation to crossfunctional teams • Oversight of safety surveillance and pharmacovigilance activities for neuroscience products in clinical trials and post marketing setting • As the PST Lead write, review and provide input on technical documen • MD / DO with 2+ years of residency with patient management experience required • Master Public Health is preferred in addition to MD / DO • Effectively analyze clinical data and epidemiological information required • Effectively write technical documents • Work collaboratively in a team environment and be self-starting and able to work independently • Ability to effectively present recommendation / opinions in group environment • Fluency, both written and oral, in English Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​ • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​ • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​ • This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.​ AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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