Part time, onsite 1-2 days a week in San Diego, must be local (~20-25 hours a week) Key Responsibilities Serve as the study lead and/or provide study management support for complex Phase 1/2a cell therapy studies where needed; oversee enrollment, maintenance, and close-out to ensure timely delivery. Oversee aspects of study management to ensure execution accuracy and high-quality data for clinical studies. Oversee work performed by CROs, study vendors, and investigative sites taking full ownership of quality and timelines. Develop critical study documents, as needed (e.g., informed consent forms, management plans, study trackers). Required Qualifications & Experience Bachelor's degree in a scientific or healthcare-related discipline with a minimum 6 years of hands-on clinical trial management experience, preferably in a pharmaceutical or biotech environment. A combination of CRO and pharma/biotech experience will be considered. Experience supporting pre-NDA programs and Phase 1 first-in-human clinical trials, including operational strategy, study oversight, monitoring, and close-out activities. Pay $75-85/hr based on level/experience