Drug Safety Coordinator managing clinical information compliance and reporting at Cencora. Collaborating with clients for data accuracy and quality checks in the pharmaceutical industry.
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 to ensure proper documentation for patient assistance and drug safety program needs
Data entry into program specific databases and Quality Management System
Sorting, filing and review of incoming faxes and documents
Assist in processing translation of documents
Perform quality check on adverse event reports as directed by the work instructions
Assist in literature search and review activities
Perform reconciliation activities with internal and external clients/partners
Conduct follow-up and clarification seeking activities as required to ensure completeness of safety reports
Requirements
Minimum college level education required
A diploma or degree with a concentration in Life Sciences is a strong asset
Knowledge of Pharmacovigilance industry is an asset
Adaptability to change and to learn new skills as required
Experience in the medical and/or pharmaceutical field(s), medical terminology is an asset
Bilingual, English/French is a strong asset
Able to work any 8-hour shift between 8:00 AM-8 PM, if necessary
Benefits
medical, dental, and vision care
backup dependent care
adoption assistance
infertility coverage
family building support
behavioral health solutions
paid parental leave
paid caregiver leave
variety of training programs
professional development resources
opportunities to participate in mentorship programs
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