CellCarta
CellCarta is a global contract research organization (CRO) specializing in precision medicine and biomarker development. The company offers a range of testing services, including clinical biomarkers, genomics, proteomics, and histopathology, to support therapeutic development across various fields such as oncology, immunology, and infectious diseases. CellCarta provides advanced technologies like flow cytometry, mass spectrometry, and digital pathology solutions, alongside comprehensive bioinformatics and biostatistics support. With expertise in integrated sample management and logistics, CellCarta partners with clients to navigate the complexities of drug development and ensure effective health solutions.
CRO Laboratory • Oncology • Auto-Immune Diseases • Infectious Diseases • Neurological and Metabolic Disorders
Corporate Document Administrator
April 12
CellCarta
CellCarta is a global contract research organization (CRO) specializing in precision medicine and biomarker development. The company offers a range of testing services, including clinical biomarkers, genomics, proteomics, and histopathology, to support therapeutic development across various fields such as oncology, immunology, and infectious diseases. CellCarta provides advanced technologies like flow cytometry, mass spectrometry, and digital pathology solutions, alongside comprehensive bioinformatics and biostatistics support. With expertise in integrated sample management and logistics, CellCarta partners with clients to navigate the complexities of drug development and ensure effective health solutions.
CRO Laboratory • Oncology • Auto-Immune Diseases • Infectious Diseases • Neurological and Metabolic Disorders
📋 Description
• Aid in the preparation of training materials based on procedural and technical manual instructions • Aid in the formatting and preparation of documents for policy and procedural management • Aid in the preparation of procedural documents such as flowcharts, diagrams, working instructions and other • Aid in the harmonization efforts by consolidating documents and procedures as required based on Management priorities • Aid in uploading documents and creating courses in MasterControl • Verifying information in MasterControl • Archiving obsolete procedures in MasterControl • Attending training sessions to software (ie Master Control) • Ensure collaboration by other team members in performing tasks to address harmonization requirements
🎯 Requirements
• High school diploma required • Secondary degree in life sciences preferred • Previous industry, laboratory experience a plus • Document Management, records and controlled documents is an asset • Microsoft Office Skills (word, power point, excel) • Excellent command of English writing • Ability to adapt content to different tones, styles, and formats
🏖️ Benefits
• Competitive Wages • Vacation and Personal Days • Comprehensive Group Insurance Plans • RRSP Contribution with Employer Matching • Employee Annual Incentive Plan (EAIP) • Dialogue Telemedicine Service and Employee Assistance Program (EAP) • OPUS & Cie Contribution • Referral Program • Career Advancement Opportunities
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