Purpose
To lead Product Safety Teams (PST) and support one or more products as the PST Lead, ensuring that the safety profile of one or more products is adequately monitored and characterized throughout the product lifecycle (e.g., surveillance, signal detection and evaluation, risk management, etc.). 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.
- Responsible for safety surveillance for pharmaceutical / biological / drug‑device combination products.
- Lead, oversee, and set the strategy for key pharmacovigilance documents, including but not limited to medical safety assessments, regulatory responses, risk management plans, periodic safety reports (DSURs, PBRERs/PSURs, PADERs), etc.
- Lead and oversee safety surveillance and pharmacovigilance activities for products in clinical development and marketed products, applying current regulatory guidance as appropriate.
- Analyze and interpret aggregate safety data and communicate these analyses and interpretations to cross‑functional teams and regulatory authorities.
- Effectively and independently write, review and present technical documents.
- Responsible for implementing risk‑management strategies for assigned products.
- Proactively engage, inspire, coach and mentor team and colleagues.
Qualifications
- MD / DO with 2+ years of residency with patient‑management experience.
- Master Public Health preferred.
- 2‑5 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry.
- Effectively analyze and guide analysis of clinical data and epidemiological information.
- Effectively present recommendations / opinions in a group environment both internally and externally.
- Write, review and provide input on technical documents.
- Work collaboratively and lead cross‑functional teams.
- Fluency, both written and oral, in English.
- Evaluate and make independent decisions. Ability to work effectively in the situation of uncertainty and complexity, ability to multitask.
Additional Information
- 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.
Equal Opportunity Employer
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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This position is listed as full time and onsite.