Northwestern University
Clinical Research Project Manager
Northwestern University, Chicago, Illinois, United States, 60290
Overview
Join to apply for the
Clinical Research Project Manager
role at Northwestern University. Department: MED-Cancer Center Salary/Grade: EXS/7 Job Summary: Manages all activities associated with biomedical and/or social-behavioral research studies considered very complex by including multiple investigators, teams, sites, sub-contracts, participants, longitudinal assessments/interventions; and/or multi-million dollar budgets. Ensures completion of contract requirements and client specifications. Oversees day-to-day operations including identifying and securing needed resources; creating, implementing, monitoring, and updating project plans; facilitating meetings with appropriate parties; tracking tasks/deliverables to ensure timelines, milestones, and goals are attained; monitoring and reporting progress as appropriate; and resolving or escalating issues in a timely manner. May co-author scientific papers for presentation and publication and coordinates writing, submission and administration of grants. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) and all current local, state, and federal laws, regulations, guidance, policy and procedure developed by the NU Institutional Review Board (IRB), FDA CFR, and ICH guidelines.
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Join to apply for the
Clinical Research Project Manager
role at Northwestern University. Department: MED-Cancer Center Salary/Grade: EXS/7 Job Summary: Manages all activities associated with biomedical and/or social-behavioral research studies considered very complex by including multiple investigators, teams, sites, sub-contracts, participants, longitudinal assessments/interventions; and/or multi-million dollar budgets. Ensures completion of contract requirements and client specifications. Oversees day-to-day operations including identifying and securing needed resources; creating, implementing, monitoring, and updating project plans; facilitating meetings with appropriate parties; tracking tasks/deliverables to ensure timelines, milestones, and goals are attained; monitoring and reporting progress as appropriate; and resolving or escalating issues in a timely manner. May co-author scientific papers for presentation and publication and coordinates writing, submission and administration of grants. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) and all current local, state, and federal laws, regulations, guidance, policy and procedure developed by the NU Institutional Review Board (IRB), FDA CFR, and ICH guidelines.
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