Pharmacovigilance & Medical Info Specialist

AmerisourceBergen Corporation; United States; À distance; USD 65 000 - 90 000; Plein temps

Résumé du poste

Cencora is seeking a Pharmacovigilance Associate to support medical information inquiries and safety data management for the Innomar Strategies portfolio. You will help ensure accurate documentation, adherence to timelines, and coordination with medical affairs, regulatory, and safety teams.

The role emphasizes maintaining knowledge resources, supporting clinical services, and mentoring junior staff, with opportunities for process improvements and professional growth.

Qualifications

• Experience handling medical information inquiries and maintaining knowledge resources.
• Familiarity with pharmacovigilance processes and safety reporting.
• Strong attention to documentation, triage, and escalation workflows.

Responsabilités

• Leads resolution of routine and moderately complex medical information inquiries by applying approved content and standards.
• Reviews and maintains scientific response content and documentation records for consistency and audit readiness.
• Ensures accurate capture, triage, documentation, and escalation of adverse events and safety information within required timelines.
• Coordinates with medical affairs, regulatory, safety, and operations teams to resolve documentation needs and maintain continuity of service.
• Recommends updates to templates, checklists, and workflows to reduce errors and improve compliance.
• Mentors junior colleagues and reinforces updated procedures and documentation expectations.
• Evaluates inquiry trends and service data to identify practical improvements.

Connaissances

Medical information

Pharmacovigilance

Drug information

Clinical services

Medical affairs support

Formation

High School Diploma/GED

Associate's degree in pharmacy or related field

Description du poste

Cencora is seeking a Pharmacovigilance Associate to support medical information inquiries and safety data management for the Innomar Strategies portfolio. You will help ensure accurate documentation, adherence to timelines, and coordination with medical affairs, regulatory, and safety teams.

The role emphasizes maintaining knowledge resources, supporting clinical services, and mentoring junior staff, with opportunities for process improvements and professional growth.