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safety, clinical care and standards quality and process improvement along with all regulatory requirements for the program. Fulfills administrative duties as well as completes technical activities
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Scheduled Hours 40 Position Summary Position assists investigators as coordinator of complex clinical research studies; responsible for multiple research studies simultaneously, acting as a liaison
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multiple clinical and translational research studies while ensuring adherence to regulatory and institutional guidelines. DUTIES AND RESPONSIBILITIES Data Management 40% • Collaborate with and support
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is responsible for directing multiple projects simultaneously. REQUIRED POSITION QUALIFICATIONS A Master of Social Work Degree from a program accredited by the Council on Social Work Education AND
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matters and EE opportunities, policies, and procedures; troubleshoots emergent issues involving students and preceptors; leads the learning environment and site quality program; and manages relationships
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increased responsibility for the day-to-day conduction and oversight of multiple clinical trials. Provides oversight of administration of study medications and/or study interventions, as appropriate
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, and self. Works to execute responsibilities within a team framework using open communication. Individual will provide PRN services at multiple clinical practice locations. Job Description Primary Duties
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Multiple Sclerosis Center. This role involves working closely with 6 doctors and other clinical research staff members in advancing research related to multiple sclerosis (MS) and associated conditions
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, intellectual excitement, artistic pursuits, and natural beauty. The Department of Medicine has an outstanding opportunity for a Clinical Program Analyst to join their team. The Clinical Program Analyst will be
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of medicines. Reporting to the Associate Dean for Research and Graduate Programs, the Grants and Contracts Manager is a key member of the Dean's Office research administration team, providing pre- and post-award