Pharmacovigilance Associate
2 months ago
We are seeking a highly motivated and detail-oriented Pharmacovigilance Associate to join our team. As a key member of our Pharmacovigilance department, you will be responsible for receiving, scanning, and documenting clinical information in compliance with SOPs and applicable legislation.
Key Responsibilities- Information Management: Receive, scan, and document all pertinent clinical information in compliance with SOPs and applicable legislation.
- Medical Enquiries: Address medical enquiries with the use of approved FAQs.
- Client Communication: Work directly with internal and external clients to request additional information or clarification as necessary.
- Database Management: Review patient information in database and ensure accurate documentation as per client needs.
- Data Entry: Enter data into program-specific databases.
- Administrative Tasks: Sort and file incoming faxes and documents, and perform quality checks on adverse event reports as directed by work instructions.
- Source Data Verification: Assist with and/or perform source data verification checks.
- Education: Minimum college-level education required. A diploma or degree with a concentration in Life Sciences is a strong asset.
- Experience: Experience in Medical Information, Clinical Research, or Drug Safety, or equivalent and related experience in pharmacy or pharmaceutical fields is a strong asset.
- Knowledge: Knowledge of Pharmacovigilance industry, including up-to-date knowledge of pharmacovigilance guidelines of Health Canada, US FDA, EMEA, and ICH.
- Skills: Adaptability to change and to learn new skills as required, effective communication and interpersonal skills, and ability to consistently meet deadlines.
We offer competitive total rewards compensation, including benefit programs that are comprehensive, diverse, and designed to meet the various needs across our associate population.
Work ScheduleThis is a full-time position.
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