Publié il y a 2 heures
Pharmacovigilance Coordinator
@ Brunel
Ontario
En bref
Brunel is hiring a Pharmacovigilance Coordinator on a full-time contract ending October 2027, working remotely from Ontario or Quebec. The role monitors, documents and reports adverse events, maintains pharmacovigilance data and liaises with stakeholders on safety matters. Candidates need 3+ years in pharmacovigilance or drug safety and a science bachelor's degree.
Responsabilités :
- Monitor, document and report adverse events per regulatory guidelines
- Enter and maintain accurate pharmacovigilance data
- Liaise with internal and external stakeholders on safety inquiries
- Ensure compliance with regulations and SOPs
- Collaborate with regulatory, quality and medical affairs teams
Résumé des exigences :
- Science bachelor's degree or related field
- 3+ years in pharmacovigilance or patient/drug safety
- French/English bilingual preferred
- Strong verbal and written communication
- Exceptional attention to detail with medical and regulatory forms
- Independent and self-directed, managing competing priorities
Outils et compétences
Source et dates
Site carrière / système de candidatures · careerpage
- Date publiée par l’employeur
- 2026-11-10
- Première détection par notre source
- 2026-11-10
- Mise à jour du dossier source
- 2026-11-10
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
Détails du poste
| Niveau | Intermédiaire |
| Domaine | Recherche et sciences |
| Expérience | 3 an(s) et plus |
| Heures par semaine | 40 (estimé) |
| Déplacements | avion : aucun · route : aucun |
| Milieu de travail | Domicile |
| Position | Surtout assis |
| Exigences physiques | physique faible · ordinateur élevé |
| Langues | English, French |
| Formation | Baccalauréat (exigé) |
| Domaines d’études | Science |
Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.
Brunel
Profil d’entreprise sauvegardé
Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.
This is who we are: A powerful global network. Brunel – Connecting Specialists to Pioneering Projects.
Description complète de l’entreprise
Founded in 1975, we are a global specialist delivering customised project and workforce solutions to drive sustainable industry transformations through technology and talent. With 120+ offices and a powerful network of more than 12,000 specialists around the world, we deliver Project and Consulting Solutions, Workforce Solutions and Global Mobility Solutions that transform global projects in Renewables, Conventional Energy, Mining, Life Sciences, Future Mobility, Industrials & Technology and many other sectors.
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Founded in 1975, we are a global specialist delivering customised project and workforce solutions to drive sustainable industry transformations through technology and talent. With 120+ offices and a powerful network of more than 12,000 specialists around the world, we deliver Project and Consulting Solutions, Workforce Solutions and Global Mobility Solutions that transform global projects in Renewables…
| Champ | Valeur |
|---|---|
| Secteur | Staffing and Recruiting |
| Taille | 10,001+ employees |
| Siège social | Amsterdam |
| Type d’organisation | Public Company |
| Fondée en | 1975 |
| Spécialités | RecruitmentStaffingTraineeshipsGlobal CompanyAutomotiveLegalFinanceMarketing & CommunicationHigh-techProject management |
| Offres sur Jobsy | 82 |
| Voir la page |
Pharmacovigilance Coordinator (Contract ending October 2027)
Remote - Ontario OR Quebec
Responsibilities
- Adverse Event Management: Monitor, document, and report adverse events in compliance with regulatory guidelines.
- Data Management: Enter and maintain accurate data in pharmacovigilance systems, ensuring timely updates and reports.
- Communication: Serve as a liaison with internal and external stakeholders to address safety-related inquiries and provide updates.
- Compliance: Ensure adherence to all relevant regulations, guidelines, and standard operating procedures.
- Cross-Functional Collaboration: Work closely with cross-functional teams, including regulatory, quality assurance, and medical affairs, to align on safety processes and requirements.
Requirements
- Bachelor's Degree in Science, or related field
- Experience: 3+ years of experience in pharmacovigilance, patient/drug safety.
- Language: French/English bilingual preferred.
- Communication Skills: Strong verbal and written communication skills, with the ability to collaborate effectively across teams.
- Attention to Detail: Exceptional ability to review and process detailed medical and regulatory forms accurately.
- Independence: Self-starter with the ability to work independently and manage competing priorities.
- Tech Savvy: Comfortable using pharmacovigilance systems, data management tools, and standard office software.
- Adaptability: Ability to hit the ground running and adapt to evolving workflows and timelines.
What We OfferWhy apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We'll get you going while you get on with the job.
About Us
Brunel has a reputation for working with some of the best in the business. That's what we continually strive for. Over 45 years, we've created a global network of interesting clients and talented individuals working together through a vast array of services.
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