About this role
Entry-level drug safety coordinator role supporting pharmacovigilance activities for Cencora. Responsible for clinical information management, adverse event reporting, and quality documentation in English and French. Science background required with 6 months to 1 year experience.
Must have
Minimum science graduate with 6 months to 1 year experience
Interest to work in Drug Safety or Pharmacovigilance role
Diploma or degree with concentration in Life Sciences is strong asset
Bilingual English and French is mandatory
Knowledge of Pharmacovigilance industry is an asset
Experience in medical or pharmaceutical field is an asset
Able to work any 8-hour shift between 8:00 AM and 8:00 PM if necessary
Technologies
Responsibilities
Receive scan and document all pertinent clinical information in compliance with SOP protocol and applicable legislation
Work directly with internal and external clients to request additional information or clarification as necessary
Review patient information in database and ensure accurate documentation as per client needs
Attach Post Infusion Reports to databases for patient assistance and drug safety program needs
Perform data entry into program specific databases and Quality Management System
Sort file and review incoming faxes and documents
Assist in processing translation of documents
Perform quality check on adverse event reports as directed by work instructions
Assist in literature search and review activities
Perform reconciliation activities with internal and external clients and partners
Conduct follow-up and clarification seeking activities to ensure completeness of safety reports
May be required to be on standby or on call as part of this role
Benefits
Amenities
Recruitment process
Full time position with Cencora formerly AmerisourceBergen
Affiliated with Innomar Strategies
Daily contacts with unilingual English-speaking customers patients or peers from cross-functional teams
Company committed to equal employment opportunity and accessibility accommodations
