Description
The Study Activation Specialist manages the startup activities of proposed clinical trials, enters them into Sarah Cannon Strategic Sites’ clinical research program menus, and coordinates feasibility, planning, and implementation through site activation. The role develops relationships with sponsors, CROs, pharmaceutical companies, and industry networks; maintains study and relationship databases; markets Sarah Cannon services; tracks site metrics; and serves as the primary contact for study start-up activities. The position requires a high school diploma, knowledge of pharmaceutical and clinical research processes, occasional travel, and at least one year of customer-facing experience; healthcare, research, pharmaceutical, or marketing experience is preferred.
