Neuro PV Medical Director – Degenerative & Movement Disorders

BioSpace; North Chicago (IL); Vor Ort; USD 160.000 - 260.000; Vollzeit

Benefits dieser Stelle

PTO (paid time off)

Medical/dental/vision insurance

401(k)

Long-term incentive programs

Zusammenfassung

AbbVie is seeking a Pharmacovigilance professional to support the Product Safety Lead in overseeing safety surveillance for neuroscience products across their lifecycle. The role includes signal management, interpretation of pharmacovigilance regulations, and contributing to PV documents.

Qualified candidates hold an MD/DO with 2+ years of residency, prefer MPH, and should be able to analyze clinical data, write technical PV documents, and communicate findings to cross‑functional teams within a

Qualifikationen

• MD/DO with 2+ years of residency and patient management experience.
• Master of Public Health is preferred in addition to MD/DO.
• Strong ability to analyze clinical data and epidemiological information.
• Ability to write technical pharmacovigilance documents.
• Ability to present recommendations in group settings.

Aufgaben

• Understand and apply pharmacology and non-clinical toxicology to safety surveillance.
• Provide safety surveillance for neuroscience products across development and post‑marketing.
• Contribute to medical safety assessments, periodic safety reports, and risk management plans.
• Apply regulatory guidance for safety surveillance and PV document authorship.
• Analyze aggregate safety data and communicate results to cross‑functional teams.
• Oversee PV activities for neuroscience products in trials and post‑marketing.

Kenntnisse

Pharmacovigilance

Data analysis

Medical writing

Team collaboration

Ausbildung

MD/DO

Master of Public Health (preferred)

Jobbeschreibung

AbbVie is seeking a Pharmacovigilance professional to support the Product Safety Lead in overseeing safety surveillance for neuroscience products across their lifecycle. The role includes signal management, interpretation of pharmacovigilance regulations, and contributing to PV documents.

Qualified candidates hold an MD/DO with 2+ years of residency, prefer MPH, and should be able to analyze clinical data, write technical PV documents, and communicate findings to cross‑functional teams within a