Global Neuroimmunology Patient Safety Director

BioSpace; North Chicago (IL); On-site; USD 130,000 - 170,000; Full time

Job summary

AbbVie is seeking a Pharmacovigilance Lead to oversee safety surveillance for neuroscience products across their lifecycle, including signal management and PV document authorship. The role requires MD/DO with post-residency patient management experience and strong writing skills.

Preferred MPH, ability to work independently, and strong collaboration with cross-functional teams are essential. Fluency in English is required and the role involves regulatory-compliant PV activities, including risk

Qualifications

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

Responsibilities

• Understand and apply pharmacology, chemistry and non-clinical toxicology to safely surveil safety data.
• Provide safety surveillance for neuroscience products across clinical trials and post-marketing.
• Contribute to pharmacovigilance documents (safety assessments, PSRs, regulatory responses).
• Apply regulatory guidance to safety surveillance and PV documentation.
• Analyze and interpret aggregate safety data for cross-functional communication.
• Oversee PV activities for neuroscience products across development stages.
• Lead in writing/reviewing technical documents related to PV.

Skills

English fluency

Analytical writing

Team collaboration

Education

MD/DO

Master of Public Health

Job description

AbbVie is seeking a Pharmacovigilance Lead to oversee safety surveillance for neuroscience products across their lifecycle, including signal management and PV document authorship. The role requires MD/DO with post-residency patient management experience and strong writing skills.

Preferred MPH, ability to work independently, and strong collaboration with cross-functional teams are essential. Fluency in English is required and the role involves regulatory-compliant PV activities, including risk