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Senior Medical Director, Immunology, Global Patient Safety

AbbVie · North Chicago, IL · Full time · Research

Posted Sep 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

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.

* This hybrid role could be based at any of AbbVie's location in the US such as North Chicago, IL Cambridge, MA, Worcester, MA, Irvine, CA, San Francisco, CA or Florham, NJ The Indication Product Safety Team (PST) lead for immunology products, under the direction of the Asset PST Lead will be actively and closely collaborating with the development medical lead, setting the safety strategy for a product in a development or approved indication. Indication PST lead will be responsible to one or more indications and will support safety through the product lifecycle (e.g. surveillance, signal detection, validation and assessment, risks assessment and mitigations strategies, etc…) together with the other members of the safety team (safety scientists, safety architects, and other cross functional colleagues). The PST lead will also closely collaborate with statistical science, epidemiology, regulatory and clinical development leads as well as medical affairs colleagues to support the asset strategy in the given indication with patient safety expertise. Indication PST lead will be interpreting regulations related to pharmacovigilance supporting all patient safety activities, and will be leading the safety components of pre-NDA and NDA/sNDA submissions, regulatory responses, label and label updates, RMPs, PSURs, and IB updates. Responsibilities: • Analyze and interpret aggregate safety data and communicate these analysis and interpretation to cross-functional teams, executive leadership and externally, as needed • Lead and set the strategy for key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans, NDA/sNDA submission – safety component • Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV documents • Understanding of the relevant to the patient safety evaluations pharmacology, and non-clinical toxicology data • Effectively write, review and provide input on technical documents independently • Oversight and responsibility for leading the strategy for periodic reports (DSURs, PSURs, PADERs etc.) • Strong team player, able to adapt and work in a fast-paced environment • Responsible for safety surveillance for pharmaceutical / biological / drug –device combined products • Responsible for implementing risk management strategies for assigned products • Proactively engaging, inspiring, coaching and mentoring team and colleagues • Opportunities to co-author publications and participate in initiatives to continue developing and growing as a safety leader • Significant Work Activities -Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) • MD / DO with 2+ years of patient management experience required • 5+ years of patient safety experience in the pharmaceutical industry, including relevant leadership experience • Prior involvement in marketing authorization application submissions or other relevant regulatory interactions • Prior experience in pharmaceuticals’ clinical development • Immunology/Internal medicine experience is strongly preferred • Effectively analyze and guide analysis of clinical data and epidemiological information • Effectively present recommendations / opinions in group environment both internally and externally • Write, review and provide input on technical documents • Work collaboratively and lead cross-functional teams • Ability to lead cross-functional teams in a collaborative environment 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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