Publié il y a 5 jours
Research Manager
@ Canadian Myeloma Research Group
Vaughan, Ontario
Responsabilités :
- Lead integrated planning and delivery across clinical trials, the national registry, and the biobank.
- Supervise the research roles, set priorities, allocate capacity, and resolve cross-program dependencies.
- Manage portfolio budgets, milestones, resource plans, partner commitments, and operational risks with the Chief Executive Officer and Office Manager.
- Work with the Chief Medical Officer/Medical Monitor on scientific priorities, protocol review, participant safety, and investigator engagement; preserve the…
- Oversee consent-aligned data and specimen workflows with the Data Manager, Regulatory Associate, and Biobank Manager.
- Ensure the Project Manager leads trial delivery while the Clinical Research Associate provides execution support.
Résumé des exigences :
- Education and experience requirements: Masters Degree in life sciences, clinical research, public health, health administration, or a related field; graduate training is an asset.
- Experience in research portfolio management, clinical trials, multidisciplinary team leadership, budgets, governance, and cross-platform delivery is preferred.
- Travel requirement: up to 50% travel for clinical-site engagement, monitoring visits, partner and investigator meetings, research conferences, and governance sessions.
Outils et compétences
Source et dates
Type de source non vérifié · apify-linkedin
- Date publiée par l’employeur
- 2026-11-05
- 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.
Canadian Myeloma Research Group
| Champ | Valeur |
|---|---|
| Offres sur Jobsy | 1 |
Title: Research Manager
Position type: Full-time, permanent research leadership role
Salary range: CAD $75,000–$95,000 annually (planning band; subject to validation and approval)
Reports to: Chief Executive Officer
Location and hours: Hybrid role based in Ontario/GTA, working Monday to Friday, 8:00 a.m. to 4:00 p.m., with flexibility for site and partner meetings, portfolio deadlines, and urgent research issues.
Education and experience requirements: Masters Degree in life sciences, clinical research, public health, health administration, or a related field; graduate training is an asset. Experience in research portfolio management, clinical trials, multidisciplinary team leadership, budgets, governance, and cross-platform delivery is preferred.
Role and responsibilities:
- Lead integrated planning and delivery across clinical trials, the national registry, and the biobank.
- Supervise the research roles, set priorities, allocate capacity, and resolve cross-program dependencies.
- Manage portfolio budgets, milestones, resource plans, partner commitments, and operational risks with the Chief Executive Officer and Office Manager.
- Work with the Chief Medical Officer/Medical Monitor on scientific priorities, protocol review, participant safety, and investigator engagement; preserve the distinction between medical oversight and operational line management.
- Oversee consent-aligned data and specimen workflows with the Data Manager, Regulatory Associate, and Biobank Manager.
- Ensure the Project Manager leads trial delivery while the Clinical Research Associate provides execution support.
- Coordinate research reporting, publications, access requests, quality improvement, and escalation of material risks to the Chief Executive Officer.
- Arrange external privacy, legal, and independent quality expertise where internal capacity or independence is insufficient.
- Lead day to day clinical trial execution responsibilities as assigned
Travel requirement: up to 50% travel for clinical-site engagement, monitoring visits, partner and investigator meetings, research conferences, and governance sessions.
Journal
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