Clinical Research

• Responsible for design and execution of assigned clinical trial activities
• Collaborate and liaise with external partners (e.g., KOLs)
• Develop Protocol and ICF documents/amendments and present these to governance committee
• Conduct literature review and submit clinical documents to TMF
• Develop site and CRA training materials and present these at SIVs and Investigator meetings
• Monitor clinical data for specific trends
• Ensure CRF design aligns with data collection in collaboration with Data Management/Programming
• Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents

Clinical Scientist, Cell Therapy

Senior Non-Clinical Biostatistician

Senior Principal Scientist, Clinical Research, HIV

Senior Clinical Research Director, Ophthalmology

Clinical Research Coordinator II – Radiology