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Posted 5 days ago

Research Manager

@ Canadian Myeloma Research Group

Vaughan, Ontario

Full-time
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SIGNALS

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…
  • 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.

Requirements summary:

  • 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.

Tools & skills

Source and dates

Source type not verified · apify-linkedin

Employer posting date
2026-11-05
First seen by our source
2026-11-10
Source record updated
2026-11-10

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Canadian Myeloma Research Group

FieldValue
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Job description

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.

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