Data coordinator Jobs

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ITR Laboratories Canada Inc. —Baie-d'urfe, QC
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- Full-time
- Bilingual
- Microsoft Word
- Microsoft Excel
- Dental care
- Paid time off
Quick apply
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Donor Database Coordinator
House of Friendship —Kitchener, ON
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Stores Inventory Coordinator
City of Winnipeg —Winnipeg, MB
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Inventory Coordinator
The Great Little Box Company Ltd —Richmond, BC
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Inventory Management Coordinator
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Tenaquip Limitee —Senneville, QC
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Revelstoke Mountain Resort —Revelstoke, BC
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Coordonnateur(trice) principal(e) – Logistique et gestion des inventaires (Ryder)/Senior Logistics and Inventory Coordinator (Ryder)
Ryder System —Longueuil, QC
- $75,000–$90,000 a year
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Parts & Inventory Coordinator - Strathmore, AB
Magnum Cementing Services LLC —Strathmore, AB
- Overtime
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Inventory Coordinator - Winter 26/27
Big White Ski Resort —Kelowna, BC
- $22 an hour
- Microsoft Word
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Toronto Zoo —Toronto, ON
- $30.12–$33.46 an hour
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Quick apply
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Parts Inventory and Procurement Coordinator
TKO Truck and Trailer inc. —Sherwood, SK
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Shipping & Inventory Coordinator
Recutify Inc. —Edmonton, AB
- Full-time
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Indigenous Research Coordinator - Data
The University of Calgary —Calgary, AB
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Data Coordinator / SEND Analyst

ITR Laboratories Canada Inc. -
Baie-d'urfe, QC

Quick apply

Job details

Permanent | Full-time
$17.95–$25.64 an hour
11 hours ago

Qualifications

Bilingual
Microsoft Word
French
Microsoft Excel
Microsoft Outlook
ACS
Filing
English
Microsoft Office
Analysis skills
Bachelor's
Data management
Document management
Communication skills
Adobe Acrobat
Time management

Full job description

Coordonnateur(trice) des données / Analyste SEND

Résumé du poste

Le ou la Coordonnateur(trice) des données / Analyste SEND est responsable de la collecte, de la compilation, de l’analyse, de la révision de la qualité et de la production de rapports portant sur les données d’études non cliniques afin de soutenir les études BPL (Bonnes pratiques de laboratoire) et non BPL. Ce poste assure la préparation précise des rapports d’études et des ensembles de données conformes à la norme SEND, conformément aux exigences réglementaires, aux normes de l’industrie et aux attentes des clients. La personne collabore avec plusieurs départements scientifiques et opérationnels, effectue la validation des données et des analyses statistiques, et contribue à la génération et à la livraison de données d’études et de soumissions SEND de haute qualité.

Exigences

Baccalauréat dans un domaine scientifique, en gestion des données ou combinaison équivalente de formation et d’expérience. Un diplôme d’AEC accompagné d’une expérience pertinente sera également considéré.
Expérience démontrée dans la gestion de grands ensembles de données.
Maîtrise de Microsoft Office (Word, Excel, Outlook) et d’Adobe Acrobat Professional.
Excellentes aptitudes en organisation, gestion documentaire et gestion du temps.
Excellentes compétences en communication écrite et verbale.
Souci du détail, avec de solides capacités d’analyse et de résolution de problèmes.
Capacité à travailler sous pression, à gérer plusieurs priorités et à respecter des échéances serrées.
Personne proactive, bien organisée et capable de travailler efficacement dans un environnement dynamique.
Maîtrise de l’anglais, tant à l’oral qu’à l’écrit; le bilinguisme (français/anglais) constitue un atout.
Connaissance des exigences des BPL, de Provantis, de SigmaStat, de SEND et des normes CDISC constitue un atout.
Intérêt pour les technologies de l’information et les systèmes de données constitue un atout.

Principales responsabilités

Compiler, examiner, analyser et gérer les données d’études provenant de services internes et de sources externes.
Générer et préparer les ensembles de données et domaines SEND conformément aux lignes directrices réglementaires, au SENDIG et aux normes CDISC.
Effectuer et documenter les contrôles de qualité afin d’assurer l’exactitude, l’exhaustivité et la conformité des données.
Soutenir la préparation, dans les délais requis et avec exactitude, des rapports d’études BPL/non BPL et des livrables SEND.
Contribuer à la présentation et à l’interprétation des résultats d’études pour leur inclusion dans les rapports d’études.
Effectuer des analyses statistiques à l’aide des logiciels appropriés, notamment SigmaStat et Provantis.
Coordonner les activités avec les équipes de toxicologie, de pathologie clinique, d’immunologie, d’assurance qualité et les autres parties prenantes afin de résoudre les problèmes liés aux données.
Répondre aux audits de l’Assurance qualité et soutenir les mesures correctives lorsque requis.
Veiller au respect des exigences spécifiques des clients et des échéanciers de projet.
Maintenir une connaissance à jour des exigences réglementaires et des normes de l’industrie en constante évolution concernant SEND et la gestion des données.
Fournir des mises à jour sur l’état d’avancement des projets à la direction et accomplir toute autre tâche connexe assignée.

Data Coordinator / SEND Analyst

Position Summary

The Data Coordinator / SEND Analyst is responsible for the collection, compilation, analysis, quality review, and reporting of nonclinical study data to support GLP and non-GLP studies. This role ensures the accurate preparation of study reports and SEND-compliant datasets in accordance with regulatory requirements, industry standards, and client expectations. Collaborates with multiple scientific and operational departments, performs data validation and statistical analyses, and supports the generation and delivery of high-quality study data and SEND submissions.

Requirements:

Bachelor’s degree in a scientific field, data management or equivalent combination of education and experience; AEC diploma and relevant experience will also be considered.
Demonstrated experience handling large datasets.
Proficient in Microsoft Office (Word, Excel, Outlook) and Adobe Acrobat Professional.
Strong organizational, record-keeping, and time management skills.
Excellent written and verbal communication skills.
Detail-oriented with strong analytical and problem-solving abilities.
Ability to work under pressure, manage multiple priorities, and meet tight deadlines.
Proactive, well-organized, and able to work effectively in a fast-paced environment.
Fluent in English (written and spoken); bilingualism (French/English) is an asset.
Knowledge of GLP requirements, Provantis, SigmaStat, SEND, and CDISC standards is an asset.
Interest in information technology and data systems is an asset.

Key Responsibilities

Compile, review, analyze, and manage study data from internal departments and external sources.
Generate and prepare SEND datasets and domains in accordance with regulatory guidelines, SENDIG, and CDISC standards.
Conduct and document quality control checks to ensure data accuracy, completeness, and compliance.
Support the timely and accurate preparation of GLP/non-GLP study reports and SEND deliverables.
Assist in the presentation and interpretation of study results for inclusion in study reports.
Perform statistical analyses using applicable software tools, including SigmaStat and Provantis.
Coordinate with Toxicology, Clinical Pathology, Immunology, Quality Assurance, and other stakeholders to resolve data-related issues.
Respond to Quality Assurance audits and support corrective actions as required.
Ensure client-specific requirements and project timelines are met.
Maintain awareness of evolving regulatory requirements and industry standards related to SEND and data management.
Provide project status updates to management and perform other related duties as assigned.

Pay: $17.95-$25.64 per hour

Benefits:

Casual dress
Dental care
On-site parking
Paid time off

Work Location: In person

Quick apply

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