Clinical Project Manager

Lead planning, execution, and delivery of clinical projects in the General Medicine portfolio, ensuring on-time, within-scope delivery and regulatory/quality compliance. Responsibilities include leading study start-up activities, defining and managing project plans (timelines, milestones, staffing, constraints), establishing reporting schedules for leadership and sponsor representatives, coordinating with internal/external teams and investigative sites, managing resources and budgets (including monthly billing and forecasting), ensuring SOP/protocol compliance, training project teams, coordinating site-level data collection, supporting Business Development through capability presentations and investigator meetings, overseeing close-out activities, and performing supervisory duties such as hiring and performance management. Requires Bachelor’s degree or equivalent in life sciences/healthcare with 1–3 years of clinical trials experience in a CRO or pharmaceutical setting; knowledge of GCP, ICH, FDA regulations; proficient with MS Word/Excel/Access/Project; and strong leadership and communication skills. Fully remote work arrangement within the United States.