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HomeCompaniesAbbvieSenior Medical Director-Late Stage Oncology

Senior Medical Director-Late Stage Oncology

Abbvie · Jersey City, NJ, United States · Hybrid · Active · $211,000–$400,500 / year · SmartRecruiters

Job facts

FieldValue
CompanyAbbvie
TitleSenior Medical Director-Late Stage Oncology
Normalized title-
Department / teamResearch
LocationJersey City, NJ, United States
Work modelHybrid / Hybrid
Employment typeFull Time
Salary$211,000–$400,500 / year
Statusactive
ATS providerSmartRecruiters
Posted / first seen2026-06-02 / 2026-06-03
Changed / last seen2026-06-03 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Abbvie.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SmartRecruiters.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Jersey City.Open
Department jobsActive postings in Research.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyAbbvie
Source78fbf4b3-4225-45c8-b041-228a3314c7ee
ATS providerSmartRecruiters

Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at  www.abbvie.com . Follow @abbvie on  X ,  Facebook ,  Instagram ,  YouTube ,  LinkedIn  and  Tik Tok . The Product Safety Team (PST) lead for late stage oncology products, under the direction of the Group Lead and TA Head will be actively and closely collaborating with the development medical lead, setting the strategy for the oncology programs. PST lead will be responsible to one or more products and will ensuring safety through the product lifecycle (e.g. surveillance, signal detection, validation and assessment, risks assessment and mitigations strategies, tox management, etc…) together with the other members of the  safety team (safety scientists, safety architects, safety PM, and other cross functional colleagues). The PST lead will also closely collaborate with a PK and toxicology leads, regulatory and clinical development leads as well as medical affairs colleagues to help guide dose selection and regimen, inclusion/exclusion criteria and safety monitoring for first for clinical trials as well as PMOS. 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. Responsibilities: Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance Responsible for safety surveillance for pharmaceutical / biological / drug –device combined products 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 Analyze and interpret aggregate safety data and communicate these analysis and interpretation to cross-functional teams, executive leadership and externally, as needed Effectively write, review and provide input on technical documents independently Oversight and responsibility for leading the strategy for periodic reports (DSURs, PSURs, PADERs etc.) 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 Strong team player, able to adapt and work in a fast pace environment Significant Work Activities -Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) MD / DO with 2+ years of internal medicine residency with patient management experience required; PhD or Clinical Pharmacology fellowship is preferred in addition to MD / DO, not required 5 - 8 years of Pharmacovigilance (PST lead role equivalent) / Clinical Development experience in the pharmaceutical industry required Oncology experience 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 short-term incentive programs. ​ 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

Full job record

Job ID386f3b94a04f8b0a18eb7f5f589ea20d83d4960c
Org ID85ca9fcd-dbd3-4f34-8622-ce60ce7ee353
Source ID78fbf4b3-4225-45c8-b041-228a3314c7ee
Board ID78fbf4b3-4225-45c8-b041-228a3314c7ee
Providersmartrecruiters
Provider Job Key3743990013419751
TitleSenior Medical Director-Late Stage Oncology
Normalized Title
Statusactive
Activeyes
Location TextJersey City, NJ, United States
DepartmentResearch
Team
Employment Typefull_time
Workplace Typehybrid
Remote Policyhybrid
CountryUnited States
RegionNJ
CityJersey City
Salary RawUSD 211000-400500 year
Salary Min211,000
Salary Max400,500
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://jobs.smartrecruiters.com/AbbVie/3743990013419751-senior-medical-director-late-stage-oncology
Apply URLhttps://jobs.smartrecruiters.com/AbbVie/3743990013419751-senior-medical-director-late-stage-oncology?oga=true
First Seen At2026-06-03 11:04:29Z
Last Seen At2026-06-06 10:45:35Z
Last Checked At2026-06-06 10:45:35Z
Last Changed At2026-06-03 11:04:29Z
Inactive At
Source Posted At2026-06-02 15:04:24Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=abbvie/date=2026-06-06/2026-06-06T10-45-26-237Z-add6ce205f3d964e8bf0951cb095a328af3cd9fe0cba97e1cc24d417318dd120.json
Event Fields
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Extensions
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Native Structured
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}
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GET https://api.bluedoor.sh/job-postings/v1/jobs/386f3b94a04f8b0a18eb7f5f589ea20d83d4960c?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/85ca9fcd-dbd3-4f34-8622-ce60ce7ee353JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/78fbf4b3-4225-45c8-b041-228a3314c7eeJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/386f3b94a04f8b0a18eb7f5f589ea20d83d4960c/eventsJSON