Monitor clinical trials across California for Parexel’s FSP team, supporting GCP compliance, site performance, and patient recruitment. The role combines site oversight with collaboration across study teams and clinical research sites.
Coordinate clinical metrics, product demonstrations, inventory, and CRM data for GE HealthCare’s medical technology operations in Salt Lake City.
Lead product marketing for Proof’s identity and transaction platform serving regulated enterprises. Drive positioning, launches, sales enablement, market insight, and team development.
Lead growth for SBNC’s AI-enabled student benefits platform through institutional sales, partnerships, and marketing. Build recurring revenue, strengthen partner success, and expand direct access for students.
United States
ColoradoManage clinical trial site operations for CPC, an academic research organization, with responsibility for compliance, monitoring, site activation, investigator records, budgets, and trial metrics.
United States
North CarolinaMonitor CNS and psychiatric clinical trials for Worldwide Clinical Trials, a global CRO. Oversee site management, regulatory compliance, data quality, and regional travel.
Support medical monitoring for Syneos Health oncology trials by reviewing clinical data, identifying safety risks, and helping study teams deliver trials. The role covers multiple indications and is remote within the United States.
United KingdomPromote personal development eLearning courses and destination events to a global audience. Generate leads, interview prospects, and support clients and colleagues.
Coordinate women’s health clinical research at UW–Madison, supporting maternal and fetal medicine and obstetrics and gynecology studies. Responsibilities include participant recruitment, data and sample handling, and multi-center study coordination.
United States
WisconsinCoordinate women’s health clinical trials at the University of Wisconsin–Madison, supporting study teams from protocol activation through close-out. The work spans participant communication, sponsor and institutional coordination, study data, and trial documentation.
