
Global Study Manager – FSP
Posted May 9

Posted May 9
This is a fully remote position, open to applicants in Canada.
• Provides operational leadership throughout the entire study lifecycle.
• Ensures the timely delivery of high-quality study data.
• Leads and coordinates the execution of global clinical trials.
• Offers quality oversight and coordination for regional and country operations.
• Acts as an essential member of the core team.
• Facilitates decision-making and collaborates closely with the Clinical Study Team Lead.
• Ensures the development of study-level plans.
• Approves and oversees drug supply management.
• Guarantees overall vendor oversight for vendors managed by SOMs.
• Reviews consolidated pre-trial assessment (PTA) reports and feasibility outputs.
• Bachelor’s of Science or Bachelor’s of Arts degree with a minimum of 7 years of pertinent operational clinical trial experience required.
• Master’s of Science or Master’s of Business Administration degree with at least 6 years of relevant operational clinical trial experience required.
• Demonstrated experience in clinical research and/or study management.
• Proven study management/leadership experience.
• Experience overseeing CROs and vendors.
• Experience managing per-subject costs, as well as vendor and ancillary monitoring cost projections and expenditures.
• Fluency in both written and spoken English is required.
• Ability to work outside of core business hours, as needed, to support global trials or initiatives.
• Willingness to travel, as necessary, including attending IMs, vendor kickoff and reset meetings, as well as client internal global or department-level meetings.
• Health insurance.
• Retirement plans.
• Paid time off.
• Flexible work arrangements.
• Professional development.
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