Job Title

ICON is hiring a Senior Clinical Project Manager with experience running full scope (start up to data-base lock) Hematology (Leukemia, Lymphoma, etc) trials in Canada. This position requires at least 7 years clinical experience with at least 3 years as a strong clinical Hematology PM (NOT a CTM) at a CRO/pharma. Must have experience managing full cross functional team oversight (ie data management, safety, Biometrics etc.) full global vendor management and full budget oversite. Direct hire, Full Time, Fully remote, no travel with pay up to $160k Canadian (No bonus) Typical Accountabilities: Responsible for full project deliverable, budget and vendor oversite. Clinical Hematology PM experience at a CRO/pharma. Managing full cross functional team oversight (ie data management, safety, Biometrics etc.) full global vendor management and full budget oversite. Lead and coordinate a cross-functional study team of experts to ensure the clinical study progress as planned driving achievement of milestones according to timelines, budget and quality standards; Lead and facilitate communication across all functions and provide guidance and support to the core and extended study team members as needed and in accordance with study-specific communication plan; For outsourced studies, be the primary point of contact for the CRO Project Manager to ensure study delivery according to agreed upon timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study; Provide input and hold accountability for the development of essential study level documents (i.e. Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)); Requirements: ~7 years clinical experience with at least 3 years as a strong clinical Hematology PM experience at a CRO/pharma/biotech. ~ Must have experience managing full cross functional team oversight (ie data management, safety, Biometrics etc.) full global vendor management and full budget oversite. ~ Extensive knowledge of clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development; ~ University degree, preferably in medical or biological sciences or discipline associated with clinical research. Advanced degree is preferred; ~ Oncology/hematology experience required