Lead clinical execution and medical monitoring as a Senior Clinical Scientist, supporting remote study delivery across complex pharmaceutical trials.
This Senior Clinical Scientist may lead or support studies according to size and complexity. The role provides scientific leadership for Clinical Trial Teams, trial design, endpoint development, and clinical protocol execution. Responsibilities span medical monitoring, safety data review, and operational collaboration with medical writing, data management, and external stakeholders.
Key Responsibilities: Lead or support studies based on size and complexity
Develop medical monitoring plans and review SAE reports
Monitor clinical data issues, laboratory reports, and safety values
Lead Clinical Trial Team scientific activities
Support database lock and protocol deviation reviews
Requirements: Seven years with BS/BA or five with MS/PhD
Two years leading Phase I-IV clinical trials
Two years of medical monitoring experience
Life Sciences degree required
Oncology experience required; IDV and GSM preferred
Apply clinical science, medical monitoring, and study leadership expertise to support rigorous trial execution and scientific delivery.

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📌 Senior Clinical Scientist Medical Monitoring (Manitoba)
🏢 Parexel
📍 Manitoba