Drug Safety Coordinator

Cencora•Quebec, ON

5d•CA$39,552 - CA$66,847•Remote

About The Position

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Cencora is a leading global pharmaceutical solutions company that is committed to improving the lives of people and animals everywhere. We connect manufacturers, providers, and patients to ensure that anyone can get the therapies they need, where and when they need them. We’re a purpose-driven organization, where all of our team members around the world are united in our responsibility to create healthier futures. We work together every day to help our partners bring their innovations to patients worldwide, creating unparalleled access and impact at the center of health.

Requirements

Minimum college level education required.
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
Ability to communicate effectively both orally and in writing
Effective interpersonal skills
Effective organizational skills; ability to multitask
Superior, proven attention to detail
Ability to consistently meet deadlines
Excellent problem-solving skills; ability to communicate and/or resolve issues effectively and efficiently
Computer skills (including knowledge of Microsoft Word, Excel, PowerPoint and other Office Programs)
Good internet required for remote work
The successful candidate may have daily contacts with unilingual English-speaking customers, patients or peers from cross-functional teams.

Nice To Haves

A diploma or degree with a concentration in Life Sciences is a strong asset

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
The Drug Safety Coordinator will also be assigned other duties and tasks as required from time to time
May be required to be on standby/on call as part of this role