
Spécialiste de la Saisie de Données, Bilingue
Posted 4 days ago

Posted 4 days ago
This is a fully remote position, open to applicants in Canada.
• Assist Cencora in delivering patient and provider support along with pharmaceutical commercialization services in Canada via Innomar Strategies.
• Support daily operations within the pharmacovigilance department under the guidance of the Assistant Manager, Pharmacovigilance.
• Collect, scan, and document pertinent clinical information in line with SOPs/protocols and relevant legislation.
• Address medical information inquiries utilizing approved FAQs.
• Collaborate with internal and external clients to gather further information or clarifications.
• Review patient data in databases to ensure the accuracy of documentation.
• Attach post-infusion reports to databases for patient-support and drug-safety program documentation.
• Input data into program-specific databases.
• Organize and classify incoming faxes and documents.
• Conduct quality checks on adverse-event reports following established work instructions.
• Perform or assist with source-data checks.
• Manage and redirect incoming calls, messages, and correspondence.
• Arrange meetings, secure rooms, and maintain updated calendars.
• Prepare standard documents, correspondence, and materials for meetings.
• Maintain filing systems, records, and administrative data.
• Coordinate routine travel, visitor arrangements, and logistical needs.
• Update trackers, logs, and standard reports.
• Elevate nonstandard requests, missing information, and processing challenges.
• Carry out other responsibilities as needed; work may occasionally require on-call or standby availability.
• A minimum of a college-level education is mandatory.
• Experience in medical information, clinical research, pharmacovigilance (drug safety), or equivalent relevant experience in pharmacy or within the pharmaceutical sector is viewed as a significant advantage.
• Familiarity with the pharmacovigilance industry, including current Health Canada, U.S. FDA, EMA, and ICH pharmacovigilance guidelines.
• Ability to adapt to changes and acquire new skills as necessary.
• Experience in the medical and/or pharmaceutical domains is considered beneficial.
• Knowledge of medical terminology is regarded as an asset.
• Strong verbal and written communication skills.
• Excellent interpersonal abilities.
• Strong organizational skills with proven attention to detail.
• Capacity to consistently meet deadlines.
• Exceptional problem-solving capabilities.
• Proficiency in Microsoft Word, Excel, PowerPoint, and other Microsoft Office applications.
• Medical, dental, and vision care.
• Backup dependent care.
• Adoption assistance.
• Infertility coverage.
• Family building support.
• Behavioral health solutions.
• Paid parental leave.
• Paid caregiver leave.
• Training programs.
• Professional development resources.
• Mentorship programs.
• Employee resource groups.
• Volunteer activities.
• Inclusive wellness resources supporting physical, emotional, financial, and social well-being.
• Reasonable accommodations during the employment process and throughout employment.
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