Medical Director, Early Pipeline, Immunology, GPS

AbbVie; North Chicago (IL); Sur place; USD 161 000 - 305 000; Plein temps

Résumé du poste

AbbVie is seeking a Medical Director, Early Pipeline in Immunology (GPS) to lead safety surveillance for early development products. You will drive evidence-based safety decisions and oversee PV activities across investigational programs.

You will integrate pharmacology, clinical data, and nonclinical toxicology to shape safety strategy, author PV documents, and guide cross-functional teams in a fast-paced, therapeutic area focused environment.

Qualifications

• MD/DO with 2+ years of residency in patient management.
• Pharmacovigilance experience in the pharmaceutical industry preferred.
• Ability to analyze preclinical, clinical, and epidemiological data.
• Ability to author and critically review technical documents.
• Fluent in English, both written and spoken.

Responsabilités

• Serves independently as the Product Safety Team Lead for one or more assigned products in early development, providing medical and strategic leadership to the Product Safety Team and driving evidence-based safety decisions.
• Integrates pharmacology, chemistry, clinical data, and nonclinical toxicology to lead safety surveillance and inform product safety strategy.
• Provides safety oversight for investigational products, contributes to PV documents including development product safety assessments, regulatory responses and risk management plans.
• Interprets and applies current regulatory guidance for safety surveillance and PV document authorship.
• Leads the analysis and interpretation of safety data and communicates conclusions to cross-functional teams and governance bodies.
• Writes, reviews and provides input on technical documents.
• Leads the strategy for Development Safety Update Reports (DSURs).
• Oversees safety surveillance and pharmacovigilance in clinical trials.
• Leads and implements risk management for assigned products.
• Supports other Product Safety Team Leads and due diligence projects.
• Interprets PV regulations to guide patient safety decisions.

Connaissances

Pharmacovigilance

Medical leadership

Safety surveillance

Cross-functional collab

English fluency

Formation

MD/DO with residency

Description du poste

Medical Director, Early Pipeline, Immunology, GPS

• Full-time
• Salary Min: 160500
• Salary Max: 305000
• Workday Global Grade: 21
• Compensation: USD 160,500 - USD 305,000 - yearly

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

Purpose:

Describe the primary goals, objectives or functions or outputs of this position.

Serve independently as the Product Safety Team Lead for one or more assigned products in early development, with accountability for leading safety surveillance, signal detection, validation, assessment, and risk management activities.

Responsibilities:

List up to 10 main responsibilities for the job. Include information about accountability and scope.

• Serves independently as the Product Safety Team Lead for one or more assigned products in early development, providing medical and strategic leadership to the Product Safety Team and driving evidence-based safety decisions.
• Integrates pharmacology, chemistry, clinical data, and nonclinical toxicology to lead safety surveillance and inform product safety strategy.
• Provides safety oversight for pharmaceutical / biological / drug –device combined investigational products, contributes to the authorship of key pharmacovigilance documents, including but not limited to, development product safety assessments, regulatory responses and risk management plans
• Interprets and applies current regulatory guidance as appropriate for safety surveillance and authorship of PV documents
• Leads the analysis and interpretation of safety data and communicates conclusions and recommendations to cross-functional teams and governance bodies.
• Effectively writes, reviews and provides input on technical documents.
• Leads the strategy for Development Safety Update Reports (DSURs)
• Oversight of safety surveillance and pharmacovigilance activities for products in clinical trials
• Leads and implements the risk management strategy for assigned products
• Supports other Product Safety Team Leads and due diligence projects as needed
• Interprets applicable pharmacovigilance regulations to guide patient safety activities and cross-functional safety decision-making.
• MD / DO with 2+ years of residency with patient management experience
• Pharmacovigilance experience in the pharmaceutical industry preferred
• Demonstrated ability to analyze and guide the analysis of preclinical, clinical, and epidemiological data.
• Demonstrated ability to author and critically review technical documents.
• Ability to formulate, clearly present, and defend medical safety assessments and recommendations to cross-functional teams and governance bodies.
• Work collaboratively in a team environment and be self-starting and able to work independently
• Fluency, both written and oral, in English

Key Stakeholders:

Group Head, Executive Medical Director, TA head, PST Lead, Analytics / Data Scientists, Project Management and Data Management, Clinical Development, Preclinical Safety, Precision Medicine, Regulatory Affairs

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable 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.

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