Lead oncology clinical science from home in Canada, applying medical monitoring and trial design expertise across sponsor-dedicated studies.
This Senior Clinical
Scientist supports oncology studies throughout clinical development. The work includes protocol development, safety assessment, clinical data interpretation, and collaboration with investigators, medical writers, and cross-functional teams. Scientific leadership supports rigorous trial execution and high-quality deliverables.
Lead or support oncology clinical studies and protocol execution Lead medical monitoring and review reliable adverse event reports Support safety and data monitoring committees Prepare regulatory, study, publication, and results documentation Bachelor's degree and seven years clinical research experience Master's degree or PhD and five years clinical research experience Two years pharmaceutical or drug development lead experience Strong oncology research and medical monitoring experience Canadian work authorization and willingness to travel up to 15% Apply oncology expertise, scientific judgment, and medical monitoring skills to advance high-quality clinical trials from home. #