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Senior Medical Director, Immunology, Global Patient Safety

AbbVie · North Chicago, IL · Full time · Other

Posted Sep 25, 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

This role leads an indication product safety team for immunology products. Walk me through leading safety for an indication.

What they are checking: Whether they have led safety for an indication themselves, owning signal decisions and strategy rather than supporting someone else's work.

You'd analyze and interpret aggregate safety data and communicate it to executives and externally. How do you explain an emerging signal to leadership without overstating or burying it?

What they are checking: Whether they can present an uncertain signal honestly to executives, neither raising false alarms nor downplaying a real risk.

You'd coach and mentor colleagues as a safety leader. How do you develop someone's judgment on causality?

What they are checking: Whether they can teach others to judge causality well, building a team that makes sound safety calls without them.

What would you do

A finding would require a label change with commercial consequences. How do you handle that?

What they are checking: Whether they will put patient safety first even when a label change hurts sales, since safety judgment must stay independent.

The posting requires a medical degree with at least two years of patient management, five or more years of pharmaceutical patient safety including leadership, and prefers immunology or internal medicine, with the role hybrid at any of several United States sites. Where do you sit, and which site?

What they are checking: Whether they meet the stated medical and safety credentials and know which site they want, since both are firm requirements.

About the work

You'd set strategy for medical safety assessments, regulatory responses and risk management plans. Walk me through building a risk management plan.

What they are checking: Whether they have actually built a risk management plan, including risks, monitoring and minimization measures, not just reviewed one.

You'd lead the strategy for development safety update reports, periodic safety reports and periodic adverse event reports. What is each actually for?

What they are checking: Whether they understand the purpose of each periodic safety report, which shows real command rather than familiarity with the names.

Immunology therapies suppress the immune system by design. How does that shape how you assess infection or malignancy signals?

What they are checking: Whether they understand that infection and cancer risks are expected with immune suppression, so causality assessment needs extra care.

You'd lead safety components of regulatory submissions and interactions. What does a health authority most want to see from the safety section?

What they are checking: Whether they know what regulators look for in a safety section, like clear data and honest risk discussion, and can deliver it.

You'd apply pharmacology and non-clinical toxicology data to patient safety evaluation. How do you use preclinical findings when a clinical signal appears?

What they are checking: Whether they can link preclinical findings to clinical signals, using all the evidence to judge whether a risk is real.

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The full job description

As published by AbbVie.

Responsible for supporting the Product Safety Leads (PST) and potentially support one or more products as the PST Lead under the direction of the Therapeutic Area (TA) Lead and Global TA Head in ensuring safety in one or more products to through surveillance, signal detection, validation and assessment. Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Responsibilities Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance • Safety surveillance for pharmaceutical / biological / drug –device combined products • Contribute to the authorship of key pharmacovigilance documents, including but not limited to, medical safety assessments, 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 cross-functional teams • Ability to effectively write, review and provide input on technical documents • Lead the strategy for periodic reports (PSUR’s, PADER’s etc.) • Oversight of safety surveillance and pharmacovigilance activities for products in clinical trials and post marketing • Lead and implement risk management strategy for assigned products • MD / DO with 2+ years of residency with patient management experience and Master Public Health is preferred in addition to MD / DO but not required • 2 – 4 years of Pharmacovigilance experience in the pharmaceutical industry • Effectively analyze and guide analysis of clinical data and epidemiological information • Effectively present recommendation / opinions in group environment • Write, review and provide input on technical documents • Self-starting and can work independently • Work collaboratively and lead cross-functional teams 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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