Publié il y a 15 jours
Evidence Delivery Associate/Manager, Medical Evidence Canada
@ Brunel
Mississauga, Ontario
En bref
Brunel is hiring an Evidence Delivery Associate/Manager for a 12-month contract in Mississauga, ON, with a hybrid arrangement. The role coordinates clinical study operations, serving as the main contact between Global, local teams and institutions, and managing protocols, study setup, drug supply, budgets and publication submissions.
Salaire :
51 $–64 $ de l’heure
Responsabilités :
- Coordinate study setup and protocol reviews with stakeholders
- Maintain studies in Veeva Clinical Vault and internal trackers
- Manage agreements, drug supply orders and adverse event reconciliation
- Process invoices in ABACUS and track study budgets
- Submit publications through iEnvision
Résumé des exigences :
- Science bachelor's degree minimum, master's or doctorate preferred
- Experience in project or clinical study management
- Knowledge of Canadian drug development and GCP/ICH
- Strong communication and cross-functional collaboration
- Autonomous, self-motivated, detail-oriented
Outils et compétences
Source et dates
Site carrière / système de candidatures · careerpage
- Date publiée par l’employeur
- 2026-10-27
- Première détection par notre source
- 2026-10-27
- Mise à jour du dossier source
- 2026-10-28
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
Détails du poste
| Niveau | Intermédiaire |
| Domaine | Opérations |
| Heures par semaine | 40 (estimé) |
| Milieu de travail | Bureau |
| Position | Surtout assis |
| Exigences physiques | physique faible · ordinateur élevé |
| Langues | English |
| Formation | Baccalauréat (exigé), Maîtrise (préféré), Doctorat (préféré) |
| 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
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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 | 95 |
| Voir la page |
Evidence Delivery Associate/Manager, Medical Evidence Canada (12-month contract)Mississauga, ON - Hybrid
Responsibilities
- Support the initial triage checklist and proposal cross-functional review by evaluating the operational feasibility (e.g., availability of funds and drug supply)
- Following study approval, serve as the main point of contact between Global, local, and the Institution (including but not limited to the Principal Investigator and study team)
- Coordinate the initial protocol review and subsequent protocol amendments with the relevant stakeholders
- Set up and maintain the study in Veeva Clinical Vault (e.g., upload files, enter information into fields, performance assessments)
- Distribution of IBs to Investigators for interventional trials
- Input regular updates into the internal study Excel trackers and support with monthly set up
- Lead the drafting and executing of confidentiality disclosure agreements, supporting administrative finalization of legal documents (e.g., accepting track changes, deleting comments), and consulting with Legal as needed
- Supporting the drafting and execution of research agreements and amendments
- Fill out forms to retrieve key information including LoA and WBS requests
- Support with adverse event reconciliation may include consultation with Patient Safety
- Obtain and/or complete necessary documentation for drug supply and submit order documents (e.g., drug order forms, supply plan)
- Schedule and facilitate meetings - take minutes for meetings where transcript is not used
- Submit invoices, enter information into the ABACUS accounting system, update internal budget tracker, and communicate any budget issues/changes with the relevant stakeholders (e.g., Finance Business Partner, Senior Marketing Manager)
- Submit publications for review using the iEnvision system and provide any follow up information requested by the Publication Coordinators
Requirements
- Bachelor's in science degree at a minimum but Master's or doctorate level preferred
- Experience in project management and/or clinical study management (e.g., operations and study design of clinical trials, drug development process in Canada, and relevant research guidelines [e.g., GCP/ICH])
- Demonstrated success in building rapport and navigating cross-functional matrixed environments by leveraging strong communication to influence or align stakeholders and foster collaboration, and advance initiatives through the organization
- Experience working alongside busy clinician scientists, asset if experience serving as a liaison of a pharmaceutical company
- Self-motivated and able to display autonomy and initiative; for instance, able to make decisions/ move actions forward without continual supervision or consultation
- Effective time management, prioritization, and organization and attention to detail to manage a dynamic and fast-paced changing environment
What We Offer
Why 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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